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Treatment of Child and Adolescent Problems
Thyroid Problems Treatment
Thyroid Disorder Treatment
Paediatric Critical Care
Treatment of Childhood Infections
Child Nutrition Management
Growth And Development Including General Paediatri
Management of New Born Care
Preimplantation Genetic Diagnosis (Pgd)
Congenital Ear Problem Treatment
Treatment of Polycystic Ovary Syndrome In Adolesce
Treatment of Thyroid Disease in Children
Cleft Lip Treatment
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Hi my daughter not eating she is 6 years Old but she is not interesting to eat anything as compare to other child Wht I dø?
Mangos are good for health or not 2 yers baby we have given to mangos then which type of health issues we have faced.
Hi, My daughter is 2 years and 8 months old. Though she is physically very active but she is not putting on weight. She eats protein diet though including dal, ragi, dry fruits etc. She is just 10.4 kg now muscles are weak. Please advice.
At a young age, it is fairly common to be afraid of math. The rational nature of numbers, multiplication tables, addition, subtraction and all that in between can admittedly be a tough thing to get on with at a tender age. But in most of the cases, this difficulty tends to improve as one attains maturity. This can be attributed to a growing familiarity with the subject and a subsequent change in the way of understanding certain things. But if your child suffers from a problem with understanding math even at a grown age, chances are he/she might be suffering from Dyscalculia- a special type of learning disorder that is characterized by a person’s inability to grasp the concepts of math or the very concept of numbers itself.
Dyscalculia generally occurs due to genetic factors. However, it is also possible to encounter this disorder if your child had suffered from significant brain injury in the past or have problems with remembering things. It is also possible to have this disorder, if your child is already suffering from Dyslexia ( a learning disorder which makes your child unable to read or understand written words).
The symptoms of Dyscalculia are as follows:
- Inability to recognize numbers and significant trouble while counting.
- Significant problems while performing basic additions, subtractions or divisions.
- Facing problems with how to use money or telling time.
- The problem with memorizing mathematical formulae or tables.
- Your child might be unable to discern exactly how to approach a math problem.
- Your child will be increasingly reluctant to go to a math class or feel tensed before math examinations.
- Inability to understand the basic functionality of numbers.
It is extremely important to remember that having this disorder does not necessarily mean your child has a bad academic record on the whole. Since this disorder can cause significant problems in the future for your child in terms of dealing with things in the real world, you should be extremely sensitive regarding its treatment.
The treatment of Dyscalculia might include:
- You should encourage your child more and more if they tend to get immensely frustrated with their math problems. If possible, try to help your child with his/ her homework.
- Strike a healthy relationship with your child. Make him realize that not being able to grasp the concept of numbers is not the end of the world. Explore his other skills. That might boost his lost confidence and might encourage him to approach math in a more efficient manner.
- You should try to make your child learn how to tell time or use money with little home exercises. If possible, try to make him learn the basic of math with daily activities like counting the number of flowers while walking down the streets.
- You must consult a specialist who will make your child learn numbers by following different modes other than writing. For example, the specialist might read a math problem to your child in order to make him understand the problem.
Hello drs. Meri bhanji 5 years ki hai use urine infection hua hai Dr. Ki dawai dilayi hai use baar baar urine aa rha hai. Aur fevar tez aa rha hai please koi adviced dijiye.
An infant is usually called a bundle of joy and with good reason. There are simple and carefree, and bring a smile to your face with their antics. However, the mood and health of an infant can be tarnished due to an issue which is known as galactosemia.
What is Galactosemia?
When a baby has galactosemia, he or she will have a problem when it comes to digesting galactose, which is something that is present not only in milk but in all milk products. Galactose is a sort of sugar, just like fructose and glucose is. As a matter of fact, lactose, which is what milk has, is, in fact, a combination of glucose and galactose. Also, when lactose is processed, it is broken down by the human body into its constituents.
The condition is something that is passed down through the genes of the parents of the baby. The condition would occur if the gene which causes a tendency for a baby to have galactosemia is present not only in one parent but both of them. A baby who has the condition will be lacking an enzyme which is known as the GALT enzyme. The enzyme could also not be functioning as it should be under normal circumstances.
When it comes to the problem, it is very important, to say the least, to detect it sooner rather than later as if there is a build-up of unprocessed galactose which is allowed to occur, it can affect the baby adversely and in some cases, it can also be threatening to the life of the baby!
How does it affect a baby?
The problems which can erupt due to galactosemia include issues which affect organs such as the brain, eyes, liver and kidneys. It is interesting to take note of the fact that these are all organs which either have something to do either processing the blood or are heavily dependent on it. While a baby is not in the position in which he or she can communicate the issues that are being faced, when keeping an eye out for galactosemia, the signs which are displayed include an irritability of the baby as well as lacking consumption of the milk of the mother.
Even though galactosemia may not be the case, a doctor should be consulted as the exacerbated issue can include seizures and jaundice. It is to be kept in mind that galactose is something that can be found not only in the milk of the cow but also human milk as well as the milk of other animals such as goats.
My child is 3 years and 2 months old and he is stutter for some times.This is continuing for past 3 months.Why he is like is this and whether he need any speech therapy or any other practice he is feeling shy for this and what is the resolution for this?
Hi, 4 months old baby admitted in NICU. Femoral vein catheterization was done. If there is oozing, leaking and edema on next day of femoral vein catheterization on right leg. Whether femoral vein catheterization was correctly inserted. How to confirm whether it was inserted correctly or not. What steps must be taken if oozing leaking and edema is there and what may be the complications. Any serious complications.Please suggest something for that.
My son is of 12 days n is yellowish on body n eyes his jaundice reports r normal then what is the reason for this. Is there any thing serious about it.
What is congenital hypothyroidism?
Newborn babies who are unable to make enough thyroid hormone have congenital hypothyroidism, meaning they are born with an underactive or absent thyroid gland. If the condition is not found and treated, children can have mental retardation and growth failure. But the good news is that early diagnosis and proper treatment can prevent these problems. In most cases, the condition is permanent and your child will need lifelong treatment.
What causes congenital hypothyroidism?
The most common causes are
- An underdeveloped thyroid gland
- A thyroid gland that’s not located where it should be (in the neck below the voice box or larynx)
- A missing thyroid gland
Other possible causes include
- Defective production of thyroid hormone (an inherited condition)
- Problems with the pituitary gland (located at the base of the brain), which tells the thyroid to make thyroid hormone
- Less commonly, a mother’s thyroid disease or medicines taken during pregnancy can cause congenital hypothyroidism.
What are the signs and symptoms of congenital hypothyroidism?
Many babies with congenital hypothyroidism appear normal at birth or for several months after birth. But others may have these signs and symptoms:
- Jaundice (yellowing of the skin and eyes)
- Poor muscle tone
- A hoarse cry
- They might also have
- Feeding problems
- A thick, large tongue
- A puffy-looking face
- A swollen abdomen, sometimes with “outpouching” of the belly button
- Large soft spots of the skull
Thyroid hormone deficiency can also occur in older babies or young children, even if test results at birth were normal.
Early diagnosis is very important. Most of the effects of hypothyroidism are easy to reverse. For this reason, doctors always ask to get screening for hypothyroidism of your newborn.
Thyroxine is usually given to treat hypothyroidism. Once the child starts taking this medicine, blood tests are regularly done to make sure thyroid hormone levels are in a normal range.
When to Contact a Medical Professional
Call your health care provider if:
- You feel your infant shows signs or symptoms of hypothyroidism
- You are pregnant and have been exposed to antithyroid drugs or procedures
If a pregnant woman takes radioactive iodine for thyroid cancer, the thyroid gland may be destroyed in the developing fetus. Infants whose mothers have taken such medicines should be observed carefully after birth for signs of hypothyroidism. Also, pregnant women should not avoid iodine-supplemented salt. If you wish to discuss about any specific problem, you can consult an endocrinologist.