نتایج جستجو برای: msud

تعداد نتایج: 148  

Journal: :Molecular genetics and metabolism 2014
Dianne M Frazier Courtney Allgeier Caroline Homer Barbara J Marriage Beth Ogata Frances Rohr Patricia L Splett Adrya Stembridge Rani H Singh

In an effort to increase harmonization of care and enable outcome studies, the Genetic Metabolic Dietitians International (GMDI) and the Southeast Regional Newborn Screening and Genetics Collaborative (SERC) are partnering to develop nutrition management guidelines for inherited metabolic disorders (IMD) using a model combining both evidence- and consensus-based methodology. The first guideline...

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 2013
Sapna Rawal Hanna Faghfoury Timo Krings

branched-chain amino acid (bCAA) metabolism that manifests in early infancy. While there is ample description of imaging features of neonates in the medical literature, the neuroimaging findings in adults have not been as well described; the disorder only rarely presents in adulthood, and children that survive beyond infancy are usually maintained on strict dietary control to prevent metabolic ...

2015
Kittiphong Thiboonboon Pattara Leelahavarong Duangrurdee Wattanasirichaigoon Nithiwat Vatanavicharn Pornswan Wasant Vorasuk Shotelersuk Suthipong Pangkanon Chulaluck Kuptanon Sumonta Chaisomchit Yot Teerawattananon Cathy Mihalopoulos

BACKGROUND Inborn errors of metabolism (IEM) are a rare group of genetic diseases which can lead to several serious long-term complications in newborns. In order to address these issues as early as possible, a process called tandem mass spectrometry (MS/MS) can be used as it allows for rapid and simultaneous detection of the diseases. This analysis was performed to determine whether newborn scr...

2008
Abeer Fareed

Alternative Names MSUD Branched-Chain Ketoaciduria Branched-Chain Alpha-Keto Acid Dehydrogenase Deficiency BCKD Deficiency Keto Acid Decarboxylase Deficiency Maple Syrup Urine Disease, Classic Maple Syrup Urine Disease, Intermediate Maple Syrup Urine Disease, Intermittent Maple Syrup Urine Disease, Thiamine-Responsive Maple Syrup Urine Disease, E3-Deficient, with Lactic Acidosis Maple Syrup Uri...

Journal: :Behavioural brain research 2012
Giselli Scaini Brena P Teodorak Isabela C Jeremias Meline O Morais Francielle Mina Diogo Dominguini Bruna Pescador Clarissa M Comim Patrícia F Schuck Gustavo C Ferreira João Quevedo Emilio L Streck

Maple syrup urine disease (MSUD) is an autosomal recessive metabolic disorder resulting from deficiency of branched-chain α-keto acid dehydrogenase complex leading to branched chain amino acids (BCAA) leucine, isoleucine, and valine accumulation as well as their corresponding transaminated branched-chain α-keto acids. MSUD patients present neurological dysfunction and cognitive impairment. Here...

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