Cargando…
The Enigmatic Genetic Landscape of Hereditary Hearing Loss: A Multistep Diagnostic Strategy in the Italian Population
Hearing loss is the most frequent sensorineural disorder, affecting approximately 1:1000 newborns. Hereditary forms (HHL) represent 50–60% of cases, highlighting the relevance of genetic testing in deaf patients. HHL is classified as non-syndromic (NSHL—70% of cases) or syndromic (SHL—30% of cases)....
Autores principales: | Spedicati, Beatrice, Santin, Aurora, Nardone, Giuseppe Giovanni, Rubinato, Elisa, Lenarduzzi, Stefania, Graziano, Claudio, Garavelli, Livia, Miccoli, Sara, Bigoni, Stefania, Morgan, Anna, Girotto, Giorgia |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10045163/ https://www.ncbi.nlm.nih.gov/pubmed/36979683 http://dx.doi.org/10.3390/biomedicines11030703 |
Ejemplares similares
-
Whole‐exome sequencing: Clinical characterization of pediatric and adult Italian patients affected by different forms of hereditary cardiovascular diseases
por: Lenarduzzi, Stefania, et al.
Publicado: (2023) -
Lights and Shadows in the Genetics of Syndromic and Non-Syndromic Hearing Loss in the Italian Population
por: Morgan, Anna, et al.
Publicado: (2020) -
Challenging Occam’s Razor: Dual Molecular Diagnoses Explain Entangled Clinical Pictures
por: Spedicati, Beatrice, et al.
Publicado: (2022) -
Puzzling Out the Genetic Architecture of Endometriosis: Whole-Exome Sequencing and Novel Candidate Gene Identification in a Deeply Clinically Characterised Cohort
por: Santin, Aurora, et al.
Publicado: (2023) -
Identifying missing pieces in color vision defects: a genome-wide association study in Silk Road populations
por: Nardone, Giuseppe Giovanni, et al.
Publicado: (2023)