Sensory Integration therapy Evaluation and Intervention in Clients With Goldenhar Syndrome : A Case Report

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Goldenhar Syndrome: A Case Report with Review

Goldenhar syndrome is a rare condition which is characterized by a multitude of anomalies involving craniofacial structures, vertebrae, internal organs and usually occurs unilaterally. The etiology of this syndrome is unclear since it varies genetically and is linked to a plethora of reasons. Herein, we report a case of Goldenhar syndrome with hemifacial microsomia and microtia along with syste...

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Goldenhar syndrome - a case report.

Goldenhar syndrome is a developmental abnormality of 1st & 2nd branchial arch involving the craniofacial microsomia with ocular & vertebral abnormality. Though most of the cases are sporadic, some familial association is also found in autosomal dominant or recessive manner. Teratogenic effect of some toxic substances may lead to the condition. Ocular abnormalities are epibulbar dermoid, lipoder...

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Goldenhar Syndrome: A rare case report

Goldenhar Syndrome or oculoauriculovertebral spectrum is a complex syndrome characterized by an association of maxillomandibular hypoplasia, deformity of the ear, ocular dermoid and vertebral anomalies and the most severe form of hemifacial microsomia. Here, we describe a 26-year-old male patient with unilateral hemifacial microsomia, preauricular ear tags, macrosomia on the right side of the f...

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Goldenhar syndrome: a case report with review of literature.

A case of Goldenhar Syndrome, in an adult male, with the typical triad of auricular appendages, epibulbar dermoid and vertebral anomalies is presented. The relevent literature is review. The differential diagnosis of this Syndrome from a few similar syndromes is stressed.

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Goldenhar Syndrome in a Nigerian Child: A Case Report

A three year old Nigerian girl presented with features suggestive of Goldenhar syndrome. The patient presented with lacrimation in the left eye and this prompted the maternal grandmother to bring the child to the hospital. No similar occurrence in the family of the patient. Multidisciplinary approach was adopted in the care of the patient. However no significant systemic abnormality was discove...

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ژورنال

عنوان ژورنال: The Journal of the Korea Contents Association

سال: 2011

ISSN: 1598-4877

DOI: 10.5392/jkca.2011.11.11.286