| Literature DB >> 8160751 |
L G Leichtman1, B Wood, R Rohn.
Abstract
We describe an infant with a unique pattern of midline defects, including anophthalmia, cleft lip and palate, macrocephaly, cutis aplasia, and micrognathia. CNS anomalies including massive hydrocephalus with destruction of most recognizable structures were observed. The infant also developed panhypopituitarism, diabetes insipidus, and a seizure disorder. We postulate that this patient could represent a more complex form of the Delleman syndrome or a new morphogenetic syndrome secondary to ventral induction with extension to the developmental fields of the first and second branchial arches.Entities:
Mesh:
Year: 1994 PMID: 8160751 DOI: 10.1002/ajmg.1320500108
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299