Accepted Articles                   Back to the articles list | Back to browse issues page

XML Print


1- Novin Genetics diagnostic laboratory, Farah Abad 4, Farah Abad Boulevard, Sari, Mazandaran, Iran
2- Radiology Department, Medical Faculty, Babol University of Medical Sciences, Babol, Mazandaran, Iran
3- Immunogenetic Research center, Molecular and Cell Biology Research Centre, Faculty of Medicine, Mazandaran University of Medical Sciences, Sari, Iran. P.O. Box. 481751665, Sari, Mazandaran, Iran, Tell : 0098-911 116 4034, Fax : 0098-151-3543087, , hashemisoteh@mazums.ac.ir
Abstract:   (106 Views)
Introduction: Laing early-onset distal myopathy is a disorder with autosomal dominant inheritance pattern caused by a mutation in MYH7 gene that encodes the human β-myosin heavy chain. Most previous studies reported this disorder with mild symptoms involving foot and hand fingers extensors as early-onset and neck flexors as late-onset symptoms. In addition, previously reported cases suffered from the same mutation is reviewed in this study.
Case presentation: Our study describes pathological, clinical, imaging and genetic findings in the first Iranian patient suffering from Laing distal myopathy. The subject is an eight-year-old-boy with a moderate phenotype, with upper and lower limbs involvement. He also shows a weakness in neck flexors, which has been previously reported in similar cases at early ages. A genetic study was done using the whole exome sequencing method. NGS findings revealed a c.4850-4852AGA deletion (p.k1617del) mutation in MYH7, which previously reported as the cause of Laing distal myopathy. This case is the first indication of Laing distal myopathy from Iran.
Conclusions: Presenting the first Iranian patient with an already known MYH7 mutation associated withLaing distal myopathy will prove previously reported heterogeneity of this disorder’s phenotype severity, morphological variation, and age of symptoms onset.
Full-Text [PDF 1255 kb]   (25 Downloads)    
Type of Study: Case Report and Review of Literature | Subject: Genetics
Received: 2019/04/10 | Accepted: 2019/07/23

Add your comments about this article : Your username or Email:
CAPTCHA

Send email to the article author


© 2019 All Rights Reserved | Journal of Pediatrics Review

Designed & Developed by : Yektaweb