fragile X syndrome
- Subj. Area:
-
V
Medicine and Care
IX Genetics, Human Reproduction and Sexuality - Ger:
- Fragiles-X-Syndrom
- Fr:
- syndrome de l'X fragile
- SN:
- A condition characterised genotypically by mutation of the X chromosome and phenotypically by cognitive impairment, hyperactivity, seizures, language delay, and enlargement of the ears, head, and testes as well as possible mental retardation (based on MeSH-2007)
- UF:
-
FRAXA syndrome
- Conc:
-
B: Fragile X syndrome
E: fragile X syndrome
I: syndrome de l'X fragile
M: Fragile X Syndrome (D005600)
