Article
Genetic diversity of Usher syndrome in Moroccan patients.
Human genetics - 7 Jan 2026
El Khair Kenza, Bousfiha Amale, Bouzidi Aymane, Amalou Ghita, Charif Majida, Charoute Hicham, El Hamouchi Adil, Bakhchane Amina, Snoussi Khalid, Hajjij Amal, Detsouli Mustapha, Benrahma Houda, Bonnet Crystel, Lenaers Guy, Petit Christine, Barakat Abdelhamid
Abstract excerpt
Usher syndrome (USH) is a rare genetic disorder accounting for almost 50% of all hereditary deaf-blindness cases. This heterogeneous, autosomal recessive condition is categorized into 3 main clinical subtypes (USH1, USH2 and USH3) and an atypical form of USH based on the severity and age of onset of the hearing loss, the absence or presence of vestibular dysfunction and the age of retinitis pigmentosa (RP) onset....
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