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Goldenhar's syndrome: a case study
Insights
Goldenhar Syndrome, a rare condition causing craniofacial and vertebral issues, can be effectively managed. Early intervention, including speech therapy, significantly improved communication skills in a young child with this syndrome.
Area of Science:
- Medical Genetics
- Developmental Pediatrics
- Speech-Language Pathology
Background:
- Goldenhar Syndrome is a rare congenital disorder characterized by craniofacial and vertebral anomalies.
- Affected individuals often present with complex medical needs and developmental challenges.
- Early identification and intervention are crucial for managing associated deficits.
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.