Goldenhar syndrome: a cause of secondary immunodeficiency?
نویسندگان
چکیده
منابع مشابه
Goldenhar syndrome: a cause of secondary immunodeficiency?
Goldenhar syndrome (GS) results from an aberrant development of the 1st and 2nd branchial arches. There is a wide range of clinical manifestations, the most common being microtia, hemifacial microsomia, epibulbar dermoids and vertebral malformations. We present two cases of GS and secondary immunodeficiency due to anatomical defects characteristic of this disorder. Case 1 (3-year-old female) av...
متن کامل[Goldenhar syndrome].
We present a report on 9 patients with Goldenhar's Syndrome, and the criteria used for the diagnosis. Familiar data and clinical characteristics. Are described and discussed with that of other authors. The medical literature about this syndrome shows a lack of uniformity on the criteria necessary to diagnose the syndrome, as well as the role of the pathogenic factors. The authors propose the ad...
متن کاملGoldenhar Syndrome
Goldenhar syndrome (Oculo-Auriculo-Vertebral Spectrum) (OAVS) is a rare congenital condition characterized by craniofacial abnormalities associated with anomalies of the spine, heart, kidney, central nervous and gastrointestinal system. Craniofacial abnormalities include the incomplete development of the eye, ear, nose, soft palate, lips and jaw. We report a case of Goldenhar syndrome in a 14-y...
متن کاملGoldenhar Syndrome – A Literature Review
Golden har syndrome is a hereditary condition which is characterized by preauricular appendages, fistulas, and epibulbar dermoids. It not only involves the facial structures, but also includes renal, genitourinary, cardiac, and skeletal anomalies. The aetiology of the syndrome is not fully understood however many hypothesis have been proposed and described. The incidence varies from 1 in 3,500 ...
متن کاملGoldenhar 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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ژورنال
عنوان ژورنال: Allergy, Asthma & Clinical Immunology
سال: 2012
ISSN: 1710-1492
DOI: 10.1186/1710-1492-8-10