Case Report: Limb-girdle Muscular Dystrophy with New Mutation in SGCB gene
Publish place: 2nd International & 10th National Neurogenetic Congress,
Publish Year: 1396
نوع سند: مقاله کنفرانسی
زبان: English
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شناسه ملی سند علمی:
NGCMED10_122
تاریخ نمایه سازی: 16 تیر 1397
Abstract:
Limb girdle muscular dystrophies (LGMDs) are a large group of genetic diseases in which there is muscleweakness and they are heterogonous diseases. The following study reports a four years female of autosomalrecessive LGMD with proximal weakness and myopathy patterns. We detected four new alternations in thispatient that was not reported for our population. One of them was important clinically that exists as unreportedhomozygous deletion encompassing exon 2 of the SGCB gene. The use of Next Generation Sequencing (NGS) inthe diagnosis of rare genetic pathologies is becoming ever more widespread in clinical practice. We used theNGS method for the first time to analysis the mutation in this family.
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Authors
Eskandar Taghizadeh
Department of Medical Genetics, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
Hamed Abdolkarimi
Department of Biology,science and Research Branch,Islamic Azad University,Tehran, Iran
Reza Boostani
Department of Neurology, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran
Ariane Sadr-Nabavi
Medical Genetic Research Center (MGRC), Scholl of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran- Dept. of Medical Genetics, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran- Academic Center for Education, Culture