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