CRIPPLING VERTIGO AND DEAFNESS WHICH HAD THE SYNDROME OF COGAN
نویسندگان
چکیده
منابع مشابه
Síndrome de Cogan Reese Cogan Reese syndrome
Estudo realizado para descrever um caso da síndrome de Cogan Reese. Paciente do sexo feminino, 55 anos, com diagnóstico de síndrome de Cogan Reese. Melhor acuidade visual de 0,67 em olho direito e 0,2 em olho esquerdo. Pelo exame biomicroscópico não se detectou anormalidades no olho direito. No olho esquerdo haviam nódulos pigmentados na superfície anterior da íris, irregularidades corneanas e ...
متن کاملCogan ' S Syndrome
CLINICAL CASE Patient: A 28 year old man, Caucasian. Chief complain 3/2000: Redness and light sensitivity in both eyes. Past ocular history: Two year history of bilateral keratitis treated with topical steroids with initial improvement and subsequently become unresponsive. Past medical history: Idiopathic hearing loss since 1996, unresponsive to systemic cyclophosphamide and high doses of predn...
متن کاملAdams Oliver Syndrome and Congenital Deafness
Admas-Oliver syndrome is a rare autosomal dominant disease of congenital development defects association with aplasia cutis. All of 81 reported cases were of 32 group families. These two cases had congenital scalp cutis aplasia with developmental defect and hypoplasia of left foot digits in case 1.Congenital deaf-mute in both can added to the past known findings in this syndrome. Thoracic defor...
متن کاملMicrocephaly, Deafness, and Renal Dysplasia: A Case of Barakat Syndrome
Background: Barakat syndrome is a rare autosomal dominant disorder characterized by hypoparathyroidism, sensorineural deafness, and renal disease, collectively known as HDR syndrome. This disease is caused by the mutation of GATA3 gene located on chromosome 10p15. GATA3 is involved in the embryonic development of kidneys, inner ears, parathyroid glands, and central nervous systems.Case report: ...
متن کاملThe cerebral angiographic findings in Cogan syndrome.
SUMMARY Cogan syndrome is an uncommon disorder of unknown etiology characterized by vestibuloauditory dysfunction and nonsyphilitic interstitial keratitis. To our knowledge, the case herein is the first report to demonstrate the cerebral angiographic findings of a patient with this syndrome.
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ژورنال
عنوان ژورنال: International Archives of Otorhinolaryngology
سال: 2012
ISSN: 1809-9777,1809-4864
DOI: 10.7162/s1809-977720120s1po-021