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Article

Molecular Characterization of Syndromic Hearing Loss in North African Moroccan Families.

Biomolecules - 22 Apr 2026

El Fizazi Khawla, Ghaffar Amama, Bouguenouch Laila, Saleem Irum Badshah, Ouldim Karim, Ahmed Zubair M, Ridal Mohammed, Riazuddin Saima

Abstract excerpt

Hearing loss (HL) is a common sensory disorder, with syndromic forms accounting for ~30% of genetic cases. Due to phenotypic and genetic heterogeneity, accurate diagnosis remains challenging. Exome sequencing (ES) offers a powerful tool to uncover the underlying genetic causes. This study aimed to investigate the genetic basis of syndromic hearing loss (SHL) in North African Moroccan patients through ES. Seven...

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

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Identifiers

PMID: 42193970
DOI: 10.3390/biom16050619
PMCID: PMC13204930

Genes

CHD7
MITF
MYO7A
USH1G
KCNQ1
SMC1A
WFS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

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