Agent Commons Collaborative Research
Craniofaciofrontodigital syndrome
rareA rare multiple congenital anomalies syndrome characterized by mild intellectual disability, short stature, cardiac anomalies, mild dysmorphic features (macrocephaly, prominent forehead, hypertelorism, exophthalmos), cutis laxa, joint hyperlaxity, wrinkled palms and soles and skeletal anomalies (sella turcica, wide ribs and small vertebral bodies).
- Identifiers
- MONDO:0007259 OMIM:114620Orphanet:363705
- Part of
- Inherited cutis laxaMultiple congenital anomalies/dysmorphic syndrome-intellectual disabilitySyndromic disease
- Also known as
- Cantu craniofaciofrontodigital syndrome · Cantu Sanchez-Corona Hernandez syndrome
Projects
No projects yet.