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Синдром мікроделеції 15q24

ORPHA:94065· ICD-10 Q93.5· 15q24 microdeletion syndrome

Визначення(English summary)

15q24 microdeletion syndrome is a rare chromosomal anomaly characterized cytogenetically by a 1.7-6.1 Mb deletion in chromosome 15q24 and clinically by pre- and post-natal growth retardation, intellectual disability, distinct facial features, and genital, skeletal, and digital anomalies.

Поширеність
<1 / 1 000 000
Успадкування
Not applicable, Unknown
Вік початку
Childhood