Синдром фронтоназальної дисплазії-роздвоєння носа та верхніх кінцівок
ORPHA:521308· ICD-10 Q87.0· Frontonasal dysplasia-bifid nose-upper limb anomalies syndrome
Визначення(English summary)
A rare syndromic frontonasal dysplasia characterized by distinctive facial dysmorphic features including hypertelorism, almond-shaped palpebral fissures, nasal deformity with creased ridge, depressed or absent tip, and asymmetry and partial absence of nasal bones, and downturned corners of the mouth. Additional reported manifestations are limb anomalies (e. g. Poland anomaly, transverse limb agenesis, and anomalies of the hands and feet, such as camptodactyly, oligodactyly, clinodactyly, and syndactyly), frontonasal encephalocele, choanal atresia, congenital renal/cardiac malformations, and corpus callosum agenesis.
- Поширеність
- <1 / 1 000 000
- Вік початку
- Infancy, Neonatal