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Rare diseases / 3-Methylcrotonyl-CoA carboxylase deficiency / Newborn screening / Methylcrotonyl-CoA carboxylase / Biotinidase deficiency / Propionic acidemia / Health / Genetic genealogy / Medical genetics


Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD)
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Document Date: 2009-02-03 16:52:02

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File Size: 18,95 KB

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City

Plymouth / /

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IndustryTerm

elevated chemicals / chemical / /

MedicalCondition

inherited organic acid disorder / seizures / frequency These disorders / vomiting / diarrhea / autosomal recessive disorder / deficiency / metabolic disorders / CoA Carboxylase Deficiency / disorders / /

Movie

What is it? / /

Organization

Organic Acidemia Association / Save Babies Through Screening Foundation / /

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Position

care physician / physician / /

ProvinceOrState

Minnesota / Pennsylvania / /

URL

http /

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