What are some rare genetic diseases in children?

Answer by  cielo (37)

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.

Answer by  KrisK99 (25)

There are many genetic diseases in children, some rarer than others. Genetic diseases are those which children inherit from their parents; some of the more common 'rare' ones include cystic fibrosis, congenital hip displacement, congenital heart abnormalities and muscular dystrophy. Rarer genetic childhood diseases can include some forms of leukaemias, diabetes, aspergers syndrome, dandy walker syndrome and fragile X syndrome.

Answer by  sarahdobsn (6)

A rare genetic disease in children is Battens disease. Also Fragile X Syndrome, Trisonomy 18, Down's Syndrome, Hemophilia, and that just names a few. There are many more that kids are faced with.

Answer by  AbdulQadir (11)

Rare Diseases Transmitted From Parents To Offspring. Include : 1. Fragile X Syndrome, 2. Tay-sacs Disease, 3. Patau Syndrome, 4. Turner's Syndrome, 5. Bloom's Syndrome, 6. Noonan's Syndrome, 7. Cri Du Chat, 8. Tuberous Sclerosis, 9. Translocation Downs Syndrome.

Answer by  VeronicaPatridge (80)

There are many genetic diseases a child might get and some include taysachs, congenital heart failure, cystic fibrosis and hemophilia are a few.

Answer by  burhankaleem (15)

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