Genetic Survey of Autosomal Recessive Peripheral Neuropathy Cases Unravels High Genetic Heterogeneity in a Turkish Cohort.
Tarih
2021Yazar
Jordanova, Albena
Durmuş, Hacer
Yapıcı, Zuhal
Parman, Yeşim
Battaloğlu, Esra
Candayan, Ayşe
Çakar, Arman
Yunisova, Gulshan
Özdağ Acarlı, Ayşe Nur
Atkinson, Derek
Topaloğlu, Pınar
Üst veri
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Background and Objectives Inherited peripheral neuropathies (IPNs) are a group of genetic disorders of the peripheral nervous system in which neuropathy is the only or the most predominant clinical feature. The most common type of IPN is Charcot-Marie-Tooth (CMT) disease. Autosomal recessive CMT (ARCMT) is generally more severe than dominant CMT and its genetic basis is poorly understood due to high clinical and genetic diversity. Here, we report clinical and genetic findings from 56 consanguineous Turkish families initially diagnosed with CMT disease.
Bağlantı
http://hdl.handle.net/20.500.12627/170278https://avesis.istanbul.edu.tr/api/publication/4adedfd3-f384-409b-adf8-0bc46c7e364c/file
https://doi.org/10.1212/nxg.0000000000000621
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