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#16
12.10.2005, 22:02
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Цитата:
Also known as: Goldenhar-Gorlin syndrome Synonyms: Auriculovertebral syndrome, branchial arches syndrome, dysplasia oculo-auricularis, facioauriculovertebral anomaly syndrome, facio-auriculovertebral anomalad, first and second branchial arch syndrome, hemifacial microsomia, hemignathia and microtia syndrome, intrauterine facial necrosis, lateral facial dysplasia, mandibulofacial dysostosis-epibulbar dermoids syndrome, necrotic facial dysplasia, oculo-auriculo-vertebral dysplasia (Gorlin), oculovertebral dysplasia, oromandibulo-otic syndrome, otofacial dysostosis, otomandibular syndrome, otomandibular facial dysmorphogenesis. Associated persons: Maurice Goldenhar Robert James Gorlin Description: The features include conjunctival dermoid cysts, auricular appendices with pretragal blind fistula. The skull may be asymmetrical with micrognathia, with other skeletal abnormalities being accessory ribs and abnormal vertebrae. Hearing defect of various degrees from near normal to severe hearing loss (conductive type); vision defect, including diplopia of various degrees. Feeding difficulty; moderate mental retardation in only 10 % of cases. A wide variety of other disorders may also occur. Aetiology unknown. Autosomal recessive or dominant inheritance is possible. Sporadic cases occur. Male-female ratio 2:1. Occurrence is estimated from 1 in every 3,000 to 1 in every 5,000 live births. When the vertebral defects and eye anomalies are present the condition is designated as the Goldenhar syndrome, when one side of a child's face is smaller or underdeveloped in comparison with the other side, it is known as hemifacial microsomia. 
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По справочникам нашла, что возможно это синдром Алажуанина. Но при этом должно быть поражение и VI пары. Этого у ребёнка нет.
Линейный вид
