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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Bibliographic Details
Main Authors: Youssef Lakhdar, Hind Abou El Houda, Houda Mounji, Mehdi Elfakiri, Youssef Rochdi, Abdeljalil Moutaouakil, Abdelaziz Raji
Format: Article
Language:English
Published: SpringerOpen 2021-11-01
Series:The Egyptian Journal of Otolaryngology
Subjects:
Online Access:https://doi.org/10.1186/s43163-021-00176-9