Frontiers in genetics · 2024
Asymmetric scapuloperoneal phenotype of MATR3-related distal myopathy: case series.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
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Murtazina Aysylu, Subbotin Dmitrii, Kuchina Anna, Gilvanova Olga, Degterev Daniil, Shchagina Olga, Cherevatova Tatiana, Bulakh Maria, Sherstyukova Darya, Ryzhkova Oksana, Kurushina Olga, Skoblov Mikhail, Borovikov Artem, Kutsev Sergey
Аннотация
Recent research has sparked a discussion on the spectrum of diseases linked to the MATR3 gene associated with amyotrophic lateral sclerosis and distal myopathy with vocal cord and pharyngeal weakness (VCPDM). To date, fewer than 50 cases of VCPDM have been reported in the literature. We aim to build upon the work of previous researchers by gathering additional information about VCPDM. In this study, we present six patients from four unrelated families affected by VCPDM. Our observations include patients exhibiting both the typical phenotype associated with MATR3-related distal myopathy and rare symptomatic manifestations of the disease. Notably, two cases presented with an asymmetric scapuloperoneal phenotype, leading in one case to an initial misdiagnosis of facioscapulohumeral muscular dystrophy.