Gene Frequencies of Methylmalonic Acidemia Disease at the Global Level and Compiling the Pathogenic Mutations in the Iranian Population

سال انتشار: 1401
نوع سند: مقاله ژورنالی
زبان: انگلیسی
مشاهده: 17

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شناسه ملی سند علمی:

JR_REMJ-11-1_003

تاریخ نمایه سازی: 28 اسفند 1402

چکیده مقاله:

Background: Methylmalonic Acidemia (MMA) is a rare autosomal recessive metabolic disorder, resulting from a genetic defect in methylmalonyl-CoA mutase (MCM) or a defect in the biosynthesis of its cofactor, adenosyl-cobalamin (AdoCbl). This disease is caused by a mutation in six main genes (MUT, MMAA, MMAB, MMADHC, MMACHC, and MCEE). In this study, we estimate MMA-disease genes frequencies at the global level and present so far reported MMA causative mutations in the Iranian population. Materials and Methods:Human Gene Mutation Database (HGMD) has been utilized to estimate MMA-disease genes frequencies. To compile MMA mutations, we systematically reviewed PubMed and magiran databases to find related articles in English and Persian language, respectively. Results: The frequencies of causative genes among MMA patients at the global level were: MUT (۶۴.۱۴%), MMACHC (۱۷.۷۴%), MMAA (۱۳.۴۸%), MMAB (۷.۱%), MMADHC (۲.۹%) and MCEE (۰.۸۵%), respectively. Until ۳۰th August ۲۰۲۳, eighteen MMA mutations were collected from the Iranian population of which ۹ mutations have been only identified in Iran and were not reported in other populations yet. Conclusions: Collection and recognition of MMA mutations in the Iranian population can be helpful for early diagnosis and treatment before the onset of neurological symptoms in newborns.

نویسندگان

Ghazaleh Malekizadeh

Department of Molecular and Cell Biology, Faculty of Science, University of Mazandaran, Babolsar, Iran

Omid Jazayeri

Department of Molecular and Cell Biology, Faculty of Science, University of Mazandaran, Babolsar, Iran

Morteza Alijanpour

Non-communicable pediatric Disease Research Center, Health Research Institute, Babol University of Medical Science, Babol, Iran

Majid Tafrihi

Department of Molecular and Cell Biology, Faculty of Science, University of Mazandaran, Babolsar, Iran

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