Синдром МЕНМО
ORPHA:85282· ICD-10 Q87.8· MEHMO syndrome
Визначення(English summary)
A rare X-linked syndromic intellectual disability characterized by mild to profound intellectual disability, microcephaly, growth delay, and hypogenitalism. Obesity, early-onset diabetes and epilepsy are more variably present.
- Поширеність
- <1 / 1 000 000
- Успадкування
- X-linked recessive
- Вік початку
- Antenatal, Infancy, Neonatal