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Синдром дуплікації Xp22.13p22.2

ORPHA:284180· ICD-10 Q99.8· Xp22.13p22.2 duplication syndrome

Визначення(English summary)

A rare syndromic intellectual disability characterized by developmental delay and intellectual disability, learning and behavioral problems, short stature, thin and sparse hair, mild dysmorphic features, tapering fingers and later onset of scoliosis, obesity and cardiovascular problems (cardiomegaly and cardiomyopathy). Females have normal intelligence.

Поширеність
<1 / 1 000 000
Успадкування
X-linked recessive
Вік початку
Infancy, Neonatal