vitalwiki

Моносомія 5p

ORPHA:281· ICD-10 Q93.4· Monosomy 5p syndrome

Визначення(English summary)

A rare developmental defect during embryogenesis, resulting from partial or total deletion of the short arm of chromosome 5, classically characterized by a high-pitched, monotone, cat-like cry (cri du chat) present since birth, associated with varying degrees of intellectual disability, developmental delay, microcephaly, and facial dysmorphism.

Поширеність
Unknown
Успадкування
Not applicable, Unknown
Вік початку
Antenatal