| Literature DB >> 2986457 |
A Richieri-Costa, G M Colletto, T R Gollop, D Masiero.
Abstract
We describe two sibs born to a consanguineous couple. Among other clinical findings both have mental retardation, short stature, facial and skeletal abnormalities characterized by hypertelorism, broad notched nasal tip, cleft lip/palate, campto-brachy-poly-syndactyly, fibular hypoplasia, and marked anomalies of foot structures. Facial signs of the reported patients resemble those present in the fronto-nasal "dysplasia" syndrome; however, the whole clinical picture in the present patients suggests a true MCA/MR syndrome, most likely inherited as an autosomal recessive trait. Clinical and genetic aspects of the present family are discussed.Entities:
Mesh:
Year: 1985 PMID: 2986457 DOI: 10.1002/ajmg.1320200409
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299