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