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What are some rare genetic diseases in children?

asked by anja (13)

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Tags:  children  disease

answers

Hutchinson-Gilford Progeria Syndrome, Fragile X syndrome, Triple X syndrome, Tuberous Sclerosis (TSC), Trisonomy 18 also known as Edwards syndrome, Trisomy 13 also known as Patau syndrome, Laurence Moon Bardet Biedl syndrome (LMBBS), Cri Du Chat (CDC), Tay-Sachs disease, Bloom's Syndrome, Noonan syndrome, Williams syndrome, and Turner syndrome are some examples.

reply
posted by cielo (27)
7 votes

1. Fragile X Syndrome occurs when x chromosome is weak or destroyed 2. Tuberous Sclerosis or tsc 3. Trisonomy 18 occurs due to third number of chromosome

5 votes

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