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Мозаїчна трисомія 8

ORPHA:96061· ICD-10 Q92.1· Mosaic trisomy 8 syndrome

Визначення(English summary)

A rare autosomal anomaly defined by the presence of three copies of chromosome 8 in some cells of the body, and clinically characterized by facial dysmorphism, typically deep palmar and plantar creases, mild intellectual deficit and joint, urinary, cardiac and skeletal anomalies.

Поширеність
Unknown
Успадкування
Not applicable, Unknown
Вік початку
Antenatal, Infancy, Neonatal