| Literature DB >> 4056086 |
Abstract
Goldenhar's Syndrome, a rare symptom complex involving craniofacial and vertebral malformations, is reviewed and a detailed case history of a 19-mo-old exhibiting the syndrome is described. This multiple-problem child exhibited a 6-mo deficit in communication skills at 12 mo of age. After 6 mo of participation in a multidisciplinary early intervention program, including speech-language therapy, the child exhibits normal language although he has articulation problems consistent with his craniofacial defects.Entities:
Mesh:
Year: 1985 PMID: 4056086 DOI: 10.1016/0021-9924(85)90028-0
Source DB: PubMed Journal: J Commun Disord ISSN: 0021-9924 Impact factor: 2.288