上埃及枫糖浆尿病的临床、生化、分子和治疗分析

IF 0.4 Q4 PEDIATRICS
Journal of pediatric genetics Pub Date : 2021-06-01 Epub Date: 2020-08-10 DOI:10.1055/s-0040-1715111
Marwa A Dahpy, Tahia H Saleem, Osama M El-Asheer, Ahmed Abd ELrasoul, Amir M Abo Elgeit
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引用次数: 0

摘要

枫糖尿病(MSUD)是一种常染色体隐性遗传代谢疾病,由任何编码支链酮脱氢酶(BCKDH)成分的基因突变引起。这项研究筛选了整个上埃及的MSUD患者,描述了他们的症状、临床和实验室结果、基因研究和治疗,并对他们的反应进行了6个月的随访。筛查发现3名儿童患有MSUD。在第二例MSUD患者中发现BCKDHA基因R195Q单核苷酸多态性(SNP)纯合突变。随访6个月以评估治疗方案和病例进展,结果表明早期治疗方案包括限制支链氨基酸饮食并给予左旋肉碱可以预防msud相关的智力残疾。结论:R195Q SNP具有致病性,可能在部分患者中引起遗传形式的MSUD。MSUD病例很少报道;因此,这些发现将对上埃及人群中MSUD的未来病例非常有用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical, Biochemical, Molecular, and Therapeutic Analysis of Maple Syrup Urine Disease in Upper Egypt.

Maple syrup urine disease (MSUD) is an autosomal recessive inherited metabolic disorder caused by mutations in any of the genes encoding for the branched-chain keto dehydrogenase (BCKDH) components. This study screened MSUD patients throughout the whole Upper Egypt describing their symptoms, clinical and laboratory findings, genetic studies, and their treatment, with a 6-month follow-up for their responses. Screening identified three children with MSUD. Homozygous mutation in R195Q single nucleotide polymorphism (SNP) within the BCKDHA gene was found with the second MSUD patient. Follow-up for 6 months to assess the treatment regimens and progression of cases demonstrated that early treatment regimens including a dietary restriction of branched-chain amino acids with L-Carnitine administration could prevent MSUD-associated intellectual disabilities. It was concluded that R195Q SNP is pathogenic, and it may cause inherited forms of MSUD in some patients. MSUD cases have rarely been reported; so these findings will be highly useful for future cases of MSUD in the Upper Egyptian population.

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来源期刊
自引率
0.00%
发文量
32
期刊介绍: The Journal of Pediatric Genetics is an English multidisciplinary peer-reviewed international journal publishing articles on all aspects of genetics in childhood and of the genetics of experimental models. These topics include clinical genetics, molecular genetics, biochemical genetics, medical genetics, dysmorphology, teratology, genetic counselling, genetic engineering, formal genetics, neuropsychiatric genetics, behavioral genetics, community genetics, cytogenetics, hereditary or syndromic cancer genetics, genetic mapping, reproductive genetics, fetal pathology and prenatal diagnosis, multiple congenital anomaly syndromes, and molecular embryology of birth defects. Journal of Pediatric Genetics provides an in-depth update on new subjects and current comprehensive coverage of the latest techniques used in the diagnosis of childhood genetics. Journal of Pediatric Genetics encourages submissions from all authors throughout the world. The following articles will be considered for publication: editorials, original and review articles, short report, rapid communications, case reports, letters to the editor, and book reviews. The aim of the journal is to share and disseminate knowledge between all disciplines in the field of pediatric genetics. This journal is a publication of the World Pediatric Society: http://www.worldpediatricsociety.org/ The Journal of Pediatric Genetics is available in print and online. Articles published ahead of print are available via the eFirst service on the Thieme E-Journals platform.
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