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Дистальна делеція 4q

ORPHA:96145· ICD-10 Q93.5· Distal deletion 4q syndrome

Визначення(English summary)

A rare partial autosomal monosomy characterized by variable combination of craniofacial, developmental, digital, skeletal, and cardiac features: hypotonia, developmental delay, growth deficiency, cleft palate, cardiovascular malformations, abnormalities of the hands and feet and typical dysmorphic features, such as microcephaly, rounded facies, small eyes, broad nasal bridge, upturned nose, full cheeks, small mouth and chin.

Вік початку
Infancy, Neonatal