Syndrome in question

dc.contributor.author	Peruzzo, Juliano	pt_BR
dc.contributor.author	Nazar, Fernanda Luca	pt_BR
dc.contributor.author	Tubone, Mariana Quirino	pt_BR
dc.contributor.author	Escobar, Gabriela Fortes	pt_BR
dc.contributor.author	Cestari, Tania Ferreira	pt_BR
dc.date.accessioned	2020-10-14T03:48:41Z	pt_BR
dc.date.issued	2015	pt_BR
dc.identifier.issn	0365-0596	pt_BR
dc.identifier.uri	http://hdl.handle.net/10183/214128	pt_BR
dc.description.abstract	Waardenburg syndrome is an inherited disease characterized by sensorineural hearing loss, pigmen-tation changes and minor facial malformations. It has four clinical variants. We report the case of a girl who, like her mother, was affected by this syndrome. The diagnosis was made after detection and treatment of deafness.	pt_BR
dc.format.mimetype	application/pdf	pt_BR
dc.language.iso	eng	pt_BR
dc.relation.ispartof	Anais brasileiros de dermatologia. Rio de Janeiro. Vol. 90, n. 4 (2015), p. 589-590	pt_BR
dc.rights	Open Access	en
dc.subject	Skin diseases, genetic	en
dc.subject	Surdez	pt_BR
dc.subject	Genetic diseases, inborn	en
dc.subject	Dermatopatias genéticas	pt_BR
dc.subject	Doenças genéticas inatas	pt_BR
dc.subject	Deafness	en
dc.subject	Síndrome de Waardenburg	pt_BR
dc.subject	Waardenburg syndrome	en
dc.title	Syndrome in question	pt_BR
dc.type	Artigo de periódico	pt_BR
dc.identifier.nrb	001117526	pt_BR
dc.type.origin	Nacional	pt_BR

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