Синдром мікробрахіцефалії-птозу-розщілини губи
ORPHA:2511· ICD-10 Q87.8· Microbrachycephaly-ptosis-cleft lip syndrome
Визначення(English summary)
Microbrachycephaly-ptosis-cleft lip syndrome is characterised by the association of intellectual deficit, microbrachycephaly, hypotelorism, palpebral ptosis, a thin/long face, cleft lip, and anomalies of the lumbar vertebra, sacrum and pelvis. It has been described in two Brazilian sisters. Transmission appears to be autosomal recessive.
- Поширеність
- <1 / 1 000 000
- Успадкування
- Autosomal recessive
- Вік початку
- Infancy, Neonatal