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Cerebral Autosomal Dominant Arteriopathy Health Feed

Last Updated: 7 years ago• Featured Tip
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DOMS

Ophthalmologist•Ahmedabad
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Are you losing your sight day by day? Does it make difficult to see you at night? Is this the onset of Blindness? Get to know about Retinitis Pigmentosa with these tips.

What actually is Retinitis Pigmentosa?
Retinitis Pigmentosa (RP) refers to a group of diseases, which causes a slow, but progressive vision loss. It is a genetic disorder that affects the ability to respond to light.This inherited disease causes a slow loss of vision, beginning with decreased night vision and loss o...more
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MD - Paediatrics, MBBS, FISPN & FISPN - ...read more

Pediatrician•Delhi
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Don't worry. You and your wife will be fine. Only thing is that she might have to undergo a cesarean section.
67 people found this helpful
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Masters

Audiologist•Gurgaon
Can not say for sure. She is not deaf. That matters. Go ahead and get married. Genetics is a complex science.
101 people found this helpful
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MD - Obstetrtics & Gynaecology, FCPS, DG...read more

Gynaecologist•Mumbai
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Little higher chances of hereditory diseases among close relatives. No more specific answers can be given unless there is some disease detected in family.
Last Updated: 7 years ago• Featured Tip
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DOMS

Ophthalmologist•Ahmedabad
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Night blindness is also called nyctalopia.It's a type of vision impairment. People with night blindness experience poor vision at night or in dimly lit environments. It is not a disease in itself, but rather a symptom of an underlying problem, usually a retina problem.

What Causes Night Blindness?
A number of eye conditions can cause night blindness, including:

Nearsightedness or blurred vision when looking at faraway objects.
Cataracts or clouding of the eye's lens.more
Asked for female, 28 years old from Bahraich
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MBBS, Diploma In Ultrasound, Fellowship ...read more

IVF Specialist•Bangalore
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The best time to get a scan that rules out congenital anamoly in foetus is 18 -24 weeks scan .Any scan done after that might have high chance of missing anamolies in the baby. That is what they have mentioned. As long as the growth of the baby in the scan you have done is adequate do not worry about the comment.
86 people found this helpful
Asked for male, 3 years old from Allahabad
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MBBS Bachelor of Medicine and Bachelor o...read more

General Physician•Raigad
Use syp Carnikid 5 ml twice a day. It's new remedy by astrum pharma for muscular dystrophies n delayed developmental problems.
87 people found this helpful
Last Updated: 7 years ago• Featured Tip
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MBBS, MD-Pediatrics, DM - Medical Geneti...read more

Geneticist•Gurgaon
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Down Syndrome is a genetic disorder resulting from chromosomal aberration. Usually, a person is born with 23 pairs of chromosomes (46 chromosomes in total). In the case of a Down Syndrome, there is a total of 47 chromosomes (an extra complete or partial chromosome appearing in the 21st pair). This extra chromosome is the main wrecker in chief that triggers the behavioral and developmental alterations characteristic of Down Syndrome.

Depending on the distribution of the chromosome during...more
Last Updated: 7 years ago• Featured Tip
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MS - Ophthalmology, MBBS

Ophthalmologist•Noida
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Refraction is a test for eye examination, which measures prescription for eyeglasses or contact lenses for individuals. The test can be performed by either an ophthalmologist or optometrist or in layman terms, an eye doctor.

Procedure for the test
In this test, the individual sits on a chair, which has a special device attached to it, called the refractor or phoropter. The individual has to look through the device and properly focus on an eye chart which is exactly 6 meters or 20 fe...more
Last Updated: 7 years ago• Featured Tip
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MBBS, MD - Obstetrtics & Gynaecology, Di...read more

Gynaecologist•Delhi
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First-trimester screening is a prenatal test. It is conducted to get early information about a baby's risk of certain chromosomal conditions. It can detect conditions like Down syndrome (trisomy 21) and extra sequences of chromosome 18 (Trisomy 18).

It is usually conducted in two steps:

Blood test
Followed by USG
Initially, a blood test is conducted to ascertain the levels of two pregnancy specific substances in the mother's blood. The blood is tested for pregnancy asso...more
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