| Literature DB >> 3201278 |
Abstract
Two female infants with Goltz syndrome (focal dermal hypoplasia) were recently investigated in the Department of Radiology, The Hospital for Sick Children, Great Ormond Street for severe feeding problems and failure to thrive. Both demonstrated severe skeletal malformations and marked gastrooesophageal reflux with laxity of the hiatus. One child (case 1) exhibited nasal regurgitation during feeding. Interestingly, both children had undergone surgery; Case 1 or a right parasagittal abdominal hernia associated with focal dermal hypoplasia of the abdominal wall and Case 2 for an exomphalos also associated with dermal hypoplasia. This observation suggests a more widespread mesodermal abnormality.Entities:
Mesh:
Year: 1988 PMID: 3201278 DOI: 10.1007/bf00364045
Source DB: PubMed Journal: Skeletal Radiol ISSN: 0364-2348 Impact factor: 2.199