Studies in Maple Syrup Urine Disease
نویسندگان
چکیده
منابع مشابه
Studies in maple syrup urine disease.
Menkes, Hurst and Craig (1954) described four infants with a progressive cerebro-degenerative disease. They were from a family of six children. Two were quite normal and of the four affected infants one survived for three months, but the others died within 14 days. An outstanding characteristic of the disease was the peculiarly pleasant smell of the urine, which was similar to that of maple syr...
متن کاملMaple syrup urine disease
Maple syrup urine disease (MSUD) is an autosomal recessive condition with an incidence of approximately 1 in 150 000 live births with a higher incidence amongst children from consanguineous relationships [1]. It is caused by an enzymatic deficiency with reduction in oxidative decarboxylation of branched-chain amino acids (BCAA) (leucine, isoleucine and valine) resulting in elevated levels and t...
متن کاملMaple Syrup Urine Disease
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...
متن کامل[Maple syrup urine disease].
Branched chain a-ketoacid dehydrogenase (BCKDH) deficiency results in maple syrup urine disease (MSUD). We examined the molecular basis of familial cases ofMSUD by analyzing the activity, subunit structure, mRNA sequence, and genome structure of the affected enzyme. The BCKDH activity in the proband with MSUD was 6% ofthe normal control level. Immunoblot analysis revealed that the ElB subunit o...
متن کاملMaple syrup urine disease
Maple syrup urine disease (MSUD) is an autosomal recessive condition with an incidence of approximately 1 in 150 000 live births with a higher incidence amongst children from consanguineous relationships [1]. It is caused by an enzymatic deficiency with reduction in oxidative decarboxylation of branched-chain amino acids (BCAA) (leucine, isoleucine and valine) resulting in elevated levels and t...
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ژورنال
عنوان ژورنال: Archives of Disease in Childhood
سال: 1961
ISSN: 0003-9888,1468-2044
DOI: 10.1136/adc.36.187.259