10664690

Source:http://linkedlifedata.com/resource/pubmed/id/10664690

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0238767, umls-concept:C0265234, umls-concept:C0395886
pubmed:issue	9
pubmed:dateCreated	2000-2-25
pubmed:abstractText	Branchio-oto-renal syndrome is a rare autosomal dominant condition characterized by hearing loss, branchial arch abnormalities and renal tract malformations. We present the first reported case of branchio-oto-renal syndrome associated with bilateral congenital cholesteatoma and ossicular chain abnormalities. The pathogenesis of this syndrome is described and the literature is reviewed.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8706896
pubmed:citationSubset	AIM
pubmed:status	MEDLINE
pubmed:month	Sep
pubmed:issn	0022-2151
pubmed:author	pubmed-author:AlbertD MDM, pubmed-author:HarcourtJJ, pubmed-author:VatsAA, pubmed-author:WorleyG AGA
pubmed:issnType	Print
pubmed:volume	113
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	841-3
pubmed:dateRevised	2005-11-16
pubmed:meshHeading	pubmed-meshheading:10664690-Branchio-Oto-Renal Syndrome, pubmed-meshheading:10664690-Cholesteatoma, Middle Ear, pubmed-meshheading:10664690-Ear Ossicles, pubmed-meshheading:10664690-Female, pubmed-meshheading:10664690-Hearing Loss, Bilateral, pubmed-meshheading:10664690-Humans, pubmed-meshheading:10664690-Infant, pubmed-meshheading:10664690-Tomography, X-Ray Computed
pubmed:year	1999
pubmed:articleTitle	Bilateral congenital cholesteatoma in branchio-oto-renal syndrome.
pubmed:affiliation	Department of Otolaryngology, Head and Neck Surgery, Great Ormond Street Hospital for Children, London, UK.
pubmed:publicationType	Journal Article, Review, Case Reports