Audiological findings of a patient with H syndrome: case report

Abstract Background H syndrome is an autosomal recessive disorder caused by mutations in SLC29A3. Hyperpigmentation, hypertrichosis, hyperglycemia, and hearing loss are some characteristics of this disorder, and it has a prevalence of < 1/1000. The aim of this report is to spread awareness among...

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Autores principales: Diala Hussein, Büşra Altın, Münir Demir Bajin
Formato: article
Lenguaje:EN
Publicado: SpringerOpen 2021
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Acceso en línea:https://doaj.org/article/1eeb8231cc54408baae4b892a3718c38
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