| Literature DB >> 6721654 |
B Lavollay, C Faure, G Filipe, G Branca, Y Huet de Barochez.
Abstract
The authors report the case of an infant presenting with a syndrome associating dwarfism, microcephaly, facial dysmorphy and important skeletal abnormalities consisting of radiologic changes concerning the skull, long bones, vertebrae, pelvis, ribs, metacarpus and metatarsus. Severe cerebral atrophy and neurologic involvement were responsible for death in the first year of life. This rare syndrome is likely to have an autosomal recessive transmission.Entities:
Mesh:
Year: 1984 PMID: 6721654
Source DB: PubMed Journal: Arch Fr Pediatr ISSN: 0003-9764