- Rett syndrome
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An inherited, neurological disease of (mostly female) children characterized by a small head, and by repetitive hand movements
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Rett syndrome
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Rett syndrome — Classification and external resources ICD 10 F84.2 ICD 9 330.8 … Wikipedia
Rett syndrome — A genetic disease that is a uniform and striking, progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. After normal development up to the age of 6 to 18 months, developmental stagnation … Medical dictionary
Rett syndrome — ▪ pathology also called cerebroatrophic hyperammonemia rare progressive neurological disorder that causes mental retardation (intellectual disability), compulsive hand movements, reduced muscle tone, difficulties in walking, autism,… … Universalium
Rett syndrome — /ˈrɛt sɪndroʊm/ (say ret sindrohm) noun a syndrome which affects girls between 6 and 18 months of age, exhibiting itself in such symptoms as social withdrawal and loss of hand coordination, and adversely affecting physical and mental development …
RTT (Rett syndrome) — A genetic disease that is a uniform and striking, progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. After normal development up to the age of 6 to 18 months, developmental stagnation … Medical dictionary
Syndrome de rett — Autre nom Aucun Référence MIM 312750 … Wikipédia en Français
Syndrome de Reth — Syndrome de Rett Syndrome de Rett Autre nom Aucun Référence MIM 312750 … Wikipédia en Français
Syndrome de Rett — Référence MIM 312750 Transmission Dominante liée à l X[1] Chromosome Xq28 Gène MECP2 … Wikipédia en Français
Rett's syndrome — or Rett syndrome ret(s) n a familial disorder that affects females usu. during infancy, that results from arrested brain development, and that is characterized by cognitive and psychomotor deterioration, dementia, stunted head growth, stereotyped … Medical dictionary
Syndrome de Prader-Willy — Syndrome de Prader Willi Syndrome de Prader Willi Autre nom Syndrome de Prader Labhart Willi Référence MIM … Wikipédia en Français
