Postnatal genetic umbilical cord analysis for earliest possible detection of inherited hearing impairment

INTRODUCTION: The most common sensorineural disorder in humans is hearing impairment and approximately 60% of prelingual hearing disorders are genetic. Especially parents with a congenital deaf child want to know as early as possible whether their second born child has the same genetic defect or not...

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Detalles Bibliográficos
Autores principales: Ketterer, Manuel Christoph, Birkenhäger, Ralf, Beck, Rainer, Arndt, Susan, Aschendorff, Antje, Kunze, Mirjam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Otology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562316/
https://www.ncbi.nlm.nih.gov/pubmed/37093292
http://dx.doi.org/10.1007/s00405-023-07986-y

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10562316/
https://www.ncbi.nlm.nih.gov/pubmed/37093292
http://dx.doi.org/10.1007/s00405-023-07986-y

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