The Tietz syndrome associated with cardiac malformation: a case report with literature review

Abstract Background Tietz syndrome is a very rare clinical entity characterized by the association of profound bilateral congenital sensorineural deafness and generalized hypopigmentation of skin, eyes, and integuments (snow white appearance). It is an autosomal dominant syndrome due to a mutation i...

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Autores principales: Youssef Lakhdar, Hind Abou El Houda, Houda Mounji, Mehdi Elfakiri, Youssef Rochdi, Abdeljalil Moutaouakil, Abdelaziz Raji
Formato: article
Lenguaje:EN
Publicado: SpringerOpen 2021
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Acceso en línea:https://doaj.org/article/a94f062046664cc5875043d58829ca9b
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