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Diagnosis And Genetic Testing for Neurological Disorder Tips

Is There A Test For Self-Assessment For Neurological Disorders?

Dr. Namit Gupta 85% (10 ratings)
MBBS, MD - Medicine, DM - Neurology
Neurologist, Gurgaon
Is There A Test For Self-Assessment For Neurological Disorders?

It is very important for any individual suffering from a neurological disorder to take medical assistance. The possible neurological condition can be diagnosed by doing some medical examinations. Some of the examinations that are conducted for diagnosis include a neurological exam, genetic screening, brain scans and many other tests.

Malfunction of the brain can be caused in more than one region of the brain like frontal cortex, anterior cingulate, Parietal cortex and Basal ganglia. It is very important that symptoms are noticed and required tests are done immediately. In case of malfunctioning in the Basal ganglia, there are chances that patients experience more anxiety and avoid clashes in life excessively.

Self - assessment test for neurological disorders

  • Self-assessment and self-administered tests can identify the presence of the neurological disorder, but it is best to seek medical assistance in such cases. The self-assessment tests can be done by an individual when they face symptoms like problems in urinating, difficulty in concentrating, problems with writing and holding objects, and experiencing blurred vision.
  • It is important for an individual facing complaints like a headache, numbness in the arms or legs, changes in behavior, fatigue, blurry vision, slurred speech, weakness and changes in coordination to contact a medical professional. The thought of neurological disorder itself is very threatening and understanding the drug options available is very important.

Medications Used
The type of medication prescribed to the patients depends mainly on the condition of the neurological disorder. Some of the drugs that are prescribed include corticosteroids. These are provided for treatment of multiple sclerosis and decrease inflammation. Levodopa is a drug used mainly for treating Parkinson’s disease. In addition to physical examination and complete medical history, the diagnostic procedures that are carried out for neurological disorders include Computer Tomography scan (CT scan), Electroencephalogram (EEG), Electromyography (EMG) and Magnetic resonance imaging (MRI).

Important Tips to Consider
The drugs used for treating neurological disorders also cause some side effects. In some cases, patients even develop a drug addiction. In such cases, the two critical components of drug addiction like withdrawal and dependence should be understood very well. Dependence on the drug occurs mainly when the patient takes the medication for a prolonged period of time. Further, depending on the nature of the medication and personal situation of the patient, addiction develops quickly. The patient tends to experience withdrawal symptoms if they become dependent on the medication and when they abruptly stop taking it. The symptoms that are caused in this situation include nausea, tremor, and headache. There are many other diagnostic tests also carried out that are useful and prevent further damage to the nervous system.

In case you have a concern or query you can always consult an expert & get answers to your questions!

3412 people found this helpful

4 Most Common Neurological Disorders You Need To Know About!

Dr. Sankalp Mohan 89% (98 ratings)
MBBS, MD - Internal Medicine, Fellow In Pain Management, DM - Neurology
Neurologist, Delhi
4 Most Common Neurological Disorders You Need To Know About!

A group of diseases which affect the brain are called neurological diseases. Any disorder which affects your brain, spine and other nerves that help in connecting both, is a neurological disorder. Neurological disorders can turn your life upside down. According to a medical survey, there are close to 600 neurological disorders which have been discovered till date. The most common neurological disorders which affect a majority of people all over the world have been listed below:

1. Alzheimer
One of the most common neurological diseases is Alzheimer. Alzheimer usually affects a large number of senior citizens on an average. However, this does not mean that individuals who are in their thirties and forties cannot be affected by this disorder. Alzheimer’s disease, also known as AD is a neurodegenerative disease which means that the disease progresses slowly and worsens over time. The life expectancy of an Alzheimer’s patient is from 3 years to 9 years after the diagnosis. Some of the commonly observed symptoms of Alzheimer’s are short-term memory loss, sudden mood swings and difficulty in speaking among others.

2. Parkinson’s disease
Another very common neurological disorder which affects a vast number of people all over the world daily is Parkinson’s disease. People affected by Parkinson’s disease or PD show symptoms much later and this is why it is difficult to detect the disorder in its early stages. Some people can get affected by Parkinson’s disease due to genetic reasons while others can be affected by certain environmental causes. People whose family members are suffering from PD are at a much higher risk of getting the disease. Some of the most common symptoms of PD are Anxiety, depression, dementia, and forgetfulness etc.

3. Migraine
A very common neurological disease which is very often taken lightly by people of all ages is a migraine. This neurological disease affects women more than men. A constant throbbing for a particular period of time on one side of your head is identified as a migraine. Some of the common symptoms of this disorder are nausea, difficulty in vision, throbbing pain in the temples or a particular side of the head, vision going black etc. Individuals who are extremely sensitive to loud noises and harsh lights, which result in severe headaches, should get themselves immediately checked.

4. Epilepsy
Epilepsy is yet another neurological disorder which is very common today. Epileptic seizures are caused by epilepsy. These seizures may last for a long while or may stop after a short period of time. The actual cause of the problem is still unknown, but you can observe symptoms like fainting, getting tremors in hands and legs or staring at a fixed spot without realization as an indication towards the disease. In case you have a concern or query you can always consult an expert & get answers to your questions!

3030 people found this helpful

Autism Spectrum Disorder - How To Diagnose It?

Dr. Gaurav Uppal 90% (357 ratings)
Diploma in Psychological Medicine, Doing Post Diploma MD, MBBS
Psychiatrist, Ludhiana
Autism Spectrum Disorder - How To Diagnose It?

Autism spectrum disorders are a group of severe neurological and developmental disorders which begin in early childhood and can last throughout a person’s life. It affects the ability to interact with others and also hinders communication and well as learning ability. A proper health center can diagnose the presence of autism spectrum disorder early on. Many tests are available for evaluation and diagnosis as it is a range of disorders which can have a variety of symptoms. The environment and genetics also play a role in the development of autism spectrum disorder but the exact cause of autism spectrum disorder is not yet known.

Symptoms of autism spectrum disorder:

  1. Your child may not be able to respond when called by his or her name by 12 months age.
  2. Will avoid eye contact and also have the desire to stay alone.
  3. Have trouble understanding or relating to other people or talk about their own feelings.
  4. Delayed speech and language skills which would affect the ability to speak.
  5. Show unusual reaction to sound, smell, taste or feelings.
  6. Answering questions with unrelated answers that have no meaning or link.
  7. Prefer to play alone and would avoid physical contact.


Diagnosis of Autism Spectrum Disorder:

  1. Comprehensive Diagnostic Evaluation – The behavior of your child and development is first studied by the doctor in detail. The tests include genetic testing, neurological testing, hearing and vision testing among others. Doctors may also suggest other specialized tests in certain cases.
  2. Developmental Screening – The development of your child’s basic learning skills with respect to the age is checked. The doctor checks for some delays in the progress and will also monitor movement, behavior and speaking progress of the child. Some additional checks are also done for low birth weight, premature birth among other things.

Treatment:

  1. Applied behavioral analysis – This is a notable treatment and widely accepted by doctors all over the world. ABA is known to encourage positive behaviors and improves a variety of skills in a child.
  2. Occupational Therapy – Teaches the skills to live independently like eating, dressing and social skills. This can help people afflicted by autism spectrum disorders to lead a normal life within the society and thus relate to as well as interact with other people.
  3. Speech therapy – It improves and focuses primarily on communication skills and also uses picture boards and gestures to improve the abilities and induce learning skills.

In case you have a concern or query you can always consult an expert & get answers to your questions!

2608 people found this helpful

How To Diagnose Sexual Dysfunction Disorder?

Gautam Clinic Pvt Ltd 91% (7785 ratings)
Sexologist Clinic
Sexologist, Faridabad
How To Diagnose Sexual Dysfunction Disorder?

Sexual dysfunction includes any problems that prevent a person or couple from achieving sexual satisfaction. Sexual dysfunction can occur at any point of the of the sexual response cycle, including arousal and desire, plateau, orgasm, and resolution. While many are shy to talk about sexual dysfunction, it’s surprisingly more common than you may think. About 31% of men experience sexual dysfunction, and 43% of women experience it.

Talk to a medical doctor if you are concerned you have a sexual dysfunction disorder in order to obtain a diagnosis and treatment.

Look into the categories of sexual disorder. While most everyone experiences nights of not being “in the mood”, disorders occur when problems occur regularly and impact the experience of sex. Think about when the problems occur and how they influence the experience of sex. The following are 4 different types of disorders:

  • Desire disorder: This occurs when you have little or no interest in sex for an ongoing amount of time. For women, things like contraceptives can greatly lower or eliminate desire.
  • Arousal disorder: Arousal disorder occurs when you want to have sex, yet your body does not respond.
  • Orgasm disorder: Your body and emotions may be engaged in sexual activity, yet you are unable to climax, which can leave you feeling frustrated.
  • Pain disorder: Pain disorder occurs when any part of sexual activity is painful, particularly intercourse.

Identify difficulties with orgasm. A lack of orgasm is called anorgasmia. Your provider may ask you questions about psychological and emotional factors that may cause anorgasmia, such as sexual inhibition, lack of experience, feelings of guilt or anxiety, or a history of sexual trauma or abuse. Some medications or chronic diseases can cause problems with arousal and orgasm.

  • Sometimes anorgasmia can be helped with sufficient stimulation.

Identify the medical causes of sexual dysfunction. Stress if often a major culprit for sexual dysfunction. However, medical and psychological factors may affect sexual satisfaction. Diagnoses such as diabetes, heart disease, neurological disorders, and hormone imbalances can also cause sexual dysfunction. Medication side-effects, drugs, and alcohol can also influence sex.

  • If you’re above the age of 65, the likelihood of experiencing lower sexual response is increased.

Discuss psychological causes. There are some sexual problems that can result from psychological causes. These can include having poor body image, mood disorders, relationship problems, or past sexual trauma.

  • Psychological causes can result in a lowered libido, decreased desire or arousal, failure to achieve orgasm, or a lack of sensitivity in the genitals.
2 people found this helpful

Cervical Cancer - Causes and Testing for Diagnosis

Panchkula & Delhi
Mother and Child Care, Panchkula
Cervical Cancer - Causes and Testing for Diagnosis

What causes cervical Cancer?

Genital Human papilloma virus (HPV) is a very common virus in both men and women that can lead to the development of genital warts, abnormal cervical cells or cervical cancer.

This virus can cause normal cells on your cervix (Know more about Cervix Infection) to turn abnormal. Over many years, abnormal cells can turn into cancer if they are not found and treated by your doctor. It can take 10 to 15 years (or more) for cells to change from normal to abnormal, and then into cancer. Abnormal cells are sometimes called 'pre cancer ' because they are not normal, but they are not yet cancer.

You cannot see or feel HPV or these cell changes on your cervix. Screening tests help us to look for these changes or for abnormal cells (Learn more about sexually transmitted diseases)

How is HPV spread?

HPV is transmitted during genital skin to-skin sexual contact. This includes vaginal or anal sex and possibly oral sex.A person can get HPV even if years have passed since he or she had sex. They will never know it because HPV usually has no signs and symptoms.

In most cases, HPV goes away within two years, without causing any health problems. It is thought that the immune system  fights off HPV infection naturally

What screening tests exist for HPV- related diseases?

Cervical Cancer: Cervical cancer can be detected with routine Cervical cancer screening (Pap test) and follow-up of abnormal results. The Pap test can find abnormal cells on the cervix so that they can be removed before cancer develops.    Abnormal cells often become normal over time, but can sometimes turn into cancer. These cells can usually be treated, depending on their severity and on the woman's age, past medical history, and other test results.

An HPV DNA test, which can find certain HPV types on a woman's cervix, may also be used with a Pap test in certain cases (called co-testing). The HPV-DNA test is done to determine if you are infected with one of the high-risk types or if your doctor finds certain type of abnormal Pap test result.

Even women who were vaccinated when they were younger need regular cervical cancer screening because the vaccines do not protect against all cervical cancer strains.

Is there a treatment for HPV or related problems?

HPV vaccination could prevent most cancers and other diseases caused by HPV. There is no treatment for the virus itself, but there are treatments for the problems that HPV can cause:

Visible genital warts may remain the same, grow more in number, or go away on their own. The warts can be treated when they appear.

Abnormal cervical cells (found on a Pap test) often become normal over time, but they can sometimes turn into cancer. If they remain abnormal, these cells can usually be treated to prevent cervical cancer from developing. This may depend on the severity of the cell changes, the woman's age , past medical history, and other test results. It is critical to follow up with testing and treatment, as recommended by a doctor.

Post detection of ovarian cancer the doctors , depending on your cancer stage can recommend the treatment more- surgery, medical treatment, radiation therapy or chemotherapy.

6767 people found this helpful

Cervical Treatment Diagnosis, Tests and Treatment

Panchkula & Delhi
Mother and Child Care, Panchkula
Cervical Treatment Diagnosis, Tests and Treatment

Cervical Cancer is most treatable when it is diagnosed and treated early. Problems found can usually be treated, depending on their severity and on the woman's age, past medical history, and other test results. Most women who get routine cervical cancer screening and follow up as told by their provider can find problems before cancer even develops. Prevention is always better than treatment.

Other HPV cancers are also more treatable when diagnosed and treated early. Although there is no routine screening test for these cancers, you should visit your doctor regularly for checkups.

Your doctor might recommend the HPV test if:

  • Your Pap test was abnormal, showing atypical squamous cells of undetermined significance (ASCUS)

  • You're age 30 or older

The HPV test is available only for women; no HPV test yet exists to detect the virus in men. However, men can be infected with HPV and pass the virus along to their sex partners.

What is a HPV Test?

The HPV test is a screening test for cervical cancer, but the test doesn't tell you whether you have cancer. Instead, the test detects the presence of HPV, the virus that causes cervical cancer, in your system. Certain types of HPV - including types 16 and 18 - increase your cervical cancer risk.

Knowing whether you have a type of HPV that puts you at high risk of cervical cancer means that you and your doctor can better decide on the next steps in your health care. Those steps might include follow-up monitoring, further testing, or treatment of abnormal or precancerous cells.

Pap- HPV Test:

HPV spreads through sexual contact and is very common in young women, so, frequently, the test results will be positive. However, HPV infections often clear on their own within a year or two. Cervical changes that lead to cancer take several years - often 10 years or more - to develop. For these reasons, you might follow a course of watchful waiting instead of undergoing treatment for cervical changes resulting from an HPV infection.

A combination Pap-HPV test is performed in your doctor's office and takes only a few minutes. You'll lie on your back on an exam table with your knees bent, your doctor will gently insert an instrument called a speculum into your vagina. The speculum holds the walls of the vagina apart and a flat scraping device called a spatula or a soft brush is used to take samples of your cervical cells. This doesn't hurt, and you may not even feel the sample being taken.

Results of your HPV test are given as positive or negative

Positive HPV test:A positive test result means that you have a type of high-risk HPV that's linked to cervical cancer. It doesn't mean that you have cervical cancer now, but it's a warning sign that cervical cancer could develop in the future. Your doctor will probably recommend a follow-up test in a year to see if the infection has cleared or to check for signs of cervical cancer.

Negative HPV test: A negative test result means that you don't have any of the types of HPV that cause cervical cancer.

Depending on your test results, your doctor may recommend one of the following as a next step:

Normal monitoring:If you're over age 30, your HPV test is negative and your Pap test normal, you'll follow the generally recommended schedule for repeating both tests in five years.

Colposcopy: In this follow-up procedure, your doctor uses a special magnifying lens (colposcope) to more closely examine your cervix.

Biopsy:In this procedure, sometimes done in conjunction with colposcopy, your doctor takes a sample of cervical cells (biopsy) to be examined more closely under a microscope.

Removal of abnormal cervical cells:To prevent abnormal cells from developing into cancerous cells, your doctor may suggest a procedure to remove the areas of tissue that contain the abnormal cells.

Seeing a specialist: If your Pap test or HPV test results are abnormal, your healthcare provider will probably refer you to a gynecologist for a colposcopic exam. If test results show that you might have cancer, you may be referred to a doctor who specializes in treating cancers of the female genital tract (gynecologic oncologist) for treatment.

If you wish to discuss about any specific problem, you can consult the doctor and ask a free question.

7229 people found this helpful

Is Gynecomastia Genetic?

Dr. Vinod Raina 89% (5866 ratings)
MD - General Medicine
Sexologist, Delhi
Is Gynecomastia Genetic?

It has been estimated that 30 to 40 percent of men will have some severity of gynecomastia in their lives. How severe it is will determine if their gynecomastia will hinder their life and be a factor in whether they need to receive treatment. Some men have a lesser severity of the condition and those around them, and themselves, may not even know it.

Determining whether you really have gynecomastia is the first step.

Gynecomastia is the over-abundance of breast tissue in a man's body causing them to develop breasts.

Pseudogynecomastia is simply a fatty layer that has built up around a man's breast, or pectoral, area.

The difference is simple to see. While gynecomastia is condition that actually is the formation of breast tissue, pseudogynecomastia is simply fat, or "man boobs", around the area that may be able to be cured with the proper exercise and diet plan.

Is Gynecomastia Genetic

Gynecomastia is genetic if it is caused by what is known as Kleinfelter Syndrome. Some facts about kleinfelter syndrome include:

  • Also known as XXY syndrome, it is present in men with an additional X chromosome.
  • While many men do not have symptoms, about 1 in every 500 men has the additional X chromosome.
  • Symptom factors depend on age at diagnosis, how many XXY cells a man may have, and the amount of testosterone in the man's body.
  • XXY men may have a taller, less muscular body when they enter puberty.
  • XXY men may have broader hips and less facial and body hair.
  • The sex lives of XXY men can be mostly normal, however they usually produce little to no sperm.

Symptoms of XXY or Kleinfelter Syndrome

  • Again, not all males with the Kleinfelter Syndrome will display symptoms.
  • As infants, XXY males may have less muscle development and less strength than those with normal genetic makeup. It is not uncommon for a XXY babies to crawl, sit-up and roll over at later stages than non-XXY males.
  • As puberty is entered, the male with Kleinfelter syndrome may not produce as much testosterone and as teens, they may have larger breasts, weaker bones and less energy.
  • In adulthood, most XXY men will look similar to others but they may be taller. Also, XXY men are more apt to health issues such as vein diseases, tooth decay, osteoporosis, and breast cancer. Autoimmune disorders are also more frequently found in men with Kleinfelter syndrome.

Treatment

There are various treatment options for males with gynecomastia due to Kleinfelter syndrome. While the XXY chromosome cannot be changed there are options to treat symptoms.

2 people found this helpful

Can You Overcome Your Genetic Risk of Heart Disease?

Dr. Pramod Kumar Sharma 93% (121 ratings)
MBBS, MS (Gen. Surgery), M.Ch - Cardio Thoracic & Vascular Surgery, DNB (CTS)
Cardiologist, Noida
Can You Overcome Your Genetic Risk of Heart Disease?

Ever wondered why you needed to share your family’s health history at a doctor’s clinic? Specific questions regarding health issues of your immediate family or close blood relatives give your doctor an insight into various health risks you might have now or in future. Those are medical conditions inherited by parents or grandparents through genes. Genes are passed from parents to children in DNA of eggs or sperms. Even a single mutation (fault) in gene can influence body systems and may lead to disorders. If any of the parents have a faulty gene, there are 50:50 chances of the child inheriting it.

Hereditary heart diseases are also a result of mutation in one or more genes and tend to run in families. Genes control almost all aspects of cardiovascular system including strengthening blood vessels, pumping capacity or communication of cells in the heart. A single genetic variation is enough to alter cardiovascular processes increasing the risk of developing a heart disease, attack or a stroke. Some of the most common hereditary cardiac disorders include; Arrhythmias, congenital heart diseases and cardiomyopathy. A family history of heart attack or stroke is also an established high-risk factor for the family members. High blood cholesterol, medically known as familial hypercholesterolemia also tends to run in families.

Unfortunately, many of these conditions cannot be prevented since they are acquired through genes. But there are many ways in which these could be managed before they become complicated or fatal.

Let’s look at some ways by which we can deal with hereditary heart diseases and increase a patient’s chances of survival:

  1. Early Diagnosis And Treatment: When one person in the family is diagnosed with a heart disease, it is strongly advisable for other family members to go in for screening. An early diagnosis can help in better treatment and management of the disease and impacts positively on patients’ life. Medical screening of siblings is highly recommended in case a person suffers a sudden cardiac death especially at a young age.

  2. Watch out for these symptoms at a young age: Abnormal heart rhythm, asthma that does not get better with inhaler, seizures that do not improve with medication, extreme fatigue or shortness of breath are warning signals and need immediate medical attention.

  3. Genetic Testing: Family members may opt for genetic testing to check if they carried genes of an inherited disorder.

  4. Genetic Counselling: Genetic counselling deals with problems like anxieties and fear of attacks, confusion over disease and emotional difficulties in accepting the situation.

We may not be able to change the family history but we can surely change our environment, lifestyle and habits. Eating healthy and following an active lifestyle does help in prevention and management of such diseases.

2154 people found this helpful

Female Genital Sores - Diagnosis and Treatment

Dr. Shantha Rama Rao 89% (108 ratings)
MD, DGO, MBBS
Gynaecologist, Chennai
Female Genital Sores - Diagnosis and Treatment

Are you experiencing swelling, bump and lesions in your vaginal area? These might be an indication of female vaginal sores. They may be itchy, quite painful, are usually tender and may also produce discharge. The sores usually develop because of skin disorders. Most cases of genital sores are symptoms of some kind sexually transmitted infection (STI). 

Diagnosis of female genital sores
A physical examination is undertaken for finding out the exact cause of genital sores and swelling in women. A pelvic test may also be carried out and you will be required to provide your doctor with your medical history reports. Blood tests, including blood work and a culture of the sore are also used for diagnosis. A culture is referred to as the method of taking a sample from your genital sore and testing it for the detection of bacteria. An ideal treatment method is suggested by your doctor after proper diagnosis. 


Treatment
There are various ways of treating vaginal sores and the exact treatment depends on the cause of the sores. Here is a list of the most common treatment methods:

 

  1. Use certain oral and topical medicines for treating the sores and getting relief from pain.
  2. Try other medicines which include pain relievers, antibiotics, corticosteroids, antiviral medications, and certain anti-itch medicines for treating vaginal sores. 
  3. Some forms of genital sores do not require treatment, but you can get rid of them if they are bothering you. A noncancerous cyst is such a type of sore.  
  4. The long term outlook for vaginal sores depends on the cause. Sores accompanied by swelling occur due to chronic skin conditions, which are likely to affect you again in the future. You should get an existing STI treated for avoiding the recurrence of vaginal sores. 
  5. The best way to keep away from vaginal sores is to have safe sex using protection, such as condoms. This will prevent the infection from being transmitted to your sexual partners. You must not hide the fact that you are having vaginal sores to avoid harassment, and should always open up and seek proper treatment.
  6. Partner should be treated. Take complete course of therapy otherwise infection may recur. Long term follow up is required in some patients.

BRCA Testing - Why Is It Required?

Dr. Mukul Gharote 90% (35 ratings)
MBBS, DM - Oncology, MD - General Medicine
Oncologist, Nashik
BRCA Testing - Why Is It Required?

The incidences of breast and ovarian cancer are on a rise. A shocking survey reveals in India, ~ 48% women with breast cancer are below the age of 50 years. The reason could be a lot of factors including lack of awareness and a delay in the diagnosis of the condition. When it comes to breast and ovarian cancer, a particular diagnostic test that has gained immense popularity over the last few years is the BRCA (BRCA1 and BRCA2) gene test. In this article, we will discuss facts related to the BRCA gene test, including its merits.

What are the BRCA genes?

The BRCA1 gene comes under the class of genes known as Tumor Suppressor Gene (antioncogene). As indicative of the name, these genes are responsible for suppressing the formation of tumors by regulating the cell division and growth, as it ensures that cell does not undergo rapid and abnormal division and proliferation. The BRCA genes also undergo mutations and modifications some of which may be harmful enough to cause cancer.

BRCA Gene Test
An early detection of breast and ovarian cancer often produces fruitful results in the successful treatment of the disorder. In the majority of the cases, genetic mutations or modifications act as a catalyst resulting in the abnormal multiplication of cells that eventually gives rise to cancer. The BRCA1 and 2 (Breast Cancer genes 1 and 2) genes play a significant role in breast and ovarian cancer. Mutation in either one of the genes (or at times both) makes a woman highly susceptible to developing breast and ovarian cancer at some point in their lives (depending on how harmful the mutation is).

  • The BRCA gene mutation is inherited and can be passed on to the subsequent generations making the situation even worse.
  • BRCA1 gene mutation may also make a person susceptible to incidences of colon and prostate cancer.
  • The BRCA gene test is basically a blood test that is carried out to find if there are any mutations (often inherited) in the BRCA1 or the BRCA2 gene.

Benefits of BRCA gene test

  • Women who have a family history of breast cancer or show signs of breast or ovarian cancer are often advised to undergo the BRCA gene test.
  • The gene test keeps a woman updated about their health status, thereby enabling them to carry out the necessary preventive measures or treatment to deal with the condition better.
  • In fact, every woman after the age of 20 should undergo the BRCA gene test.

However, there are instances (though rare) where a woman did develop breast cancer in spite of testing negative for the BRCA test indicating others gene mutations can also lead to breast cancer. In case you have a concern or query you can always consult an expert & get answers to your questions!

3143 people found this helpful
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