| Literature DB >> 2831368 |
M L Merrer1, M L Briard, S Girard, N Mulliez, C Moraine, M C Imbert.
Abstract
We report eight cases of a lethal association of failure to thrive, facial dysmorphism, ambiguous genitalia, syndactyly, postaxial polydactyly, and internal developmental anomalies (Hirschsprung's disease, cardiac and renal malformation). This syndrome is likely to be autosomal recessive and resembles Smith-Lemli-Opitz (SLO) syndrome. However, the lethality, the common occurrence of polydactyly, and the sexual ambiguity distinguishes this condition from SLO syndrome. A review of published reports supports the separate classification of this syndrome for which we propose the name lethal acrodysgenital dwarfism.Entities:
Mesh:
Year: 1988 PMID: 2831368 PMCID: PMC1015449 DOI: 10.1136/jmg.25.2.88
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318