Literature DB >> 4056086

Goldenhar's syndrome: a case study.

P Belenchia, P McCardle.   

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.

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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


  1 in total

1.  A new lumbar vertebral anomaly in Goldenhar syndrome: A case report.

Authors:  Mauro Costa Morais Tavares Junior; Dennis J Heaton; Brian M Everist; Brandon B Carlson
Journal:  Radiol Case Rep       Date:  2022-04-17
  1 in total

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