| Literature DB >> 1218241 |
J M Cantú, A Hernández, J Ramírez, M Bernal, G Rubio, J Urrusti, S Franco-Vázquez.
Abstract
Three male sibs from consanguienous parents were found to have a strikingly similar pattern of multiple congenital anomalies. The main features were polyhydramnios; low birthweight; dwarfism; epicanthal folds; abnormal ears; microretrognathia; microstomia; microglossia; glossoptosis; webbed neck; severe cardiac defects; radial and ulnar hypoplasia; radial deviation of the hands; brachymetacarpalia; thumb hypoplasia; clinodactyly and hypoplasia of the 5th finger; simian creases; fibular and tibial hypoplasia; talipes varus with hypoplastic heels; wide gap between 1st and 2nd toes; and delayed bone age. Neonatal death occurred in the 3 babies by severe cardiac failure. Differential diagnosis permits one to conclude that this is a new type of faciocardiomelic dysplasia with a probable autosomal recessive inheritance.Entities:
Mesh:
Year: 1975 PMID: 1218241
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844