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Genetic genealogy / Medical genetics / HMG-CoA / Rare diseases / Protein families / Newborn screening / Fatty-acid metabolism disorder / Health / 3-hydroxy-3-methylglutaryl-CoA lyase deficiency / 3-hydroxy-3-methylglutaryl-CoA lyase


3-Hydroxy-3-Methylglutaryl-CoA Lyase (HMG) Deficiency (metabolic condition: organic acid disorder) Also known as: • HMG-CoA lyase deficiency
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Document Date: 2013-09-16 18:32:42

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Company

St. N.W. Edmonton AB / /

Facility

Edmonton Medical Genetics Clinic / Alberta Children’s Hospital / Medical Sciences Building / /

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IndustryTerm

energy source / /

MedicalCondition

lethargy / vomiting / organic acid disorders / acid disorders / metabolic diseases / acidosis / HMG deficiency / Lyase (HMG) Deficiency / deficiency / Coma / hypoglycemia / hypotonia and enlarged liver / organic acid disorder / minor illness / /

MedicalTreatment

counselling / low fat diet / /

Organization

Alberta Children’s Hospital / /

Person

Alberta Children / /

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Position

genetic metabolic specialist / /

URL

www.albertahealthservices.ca/newbornscreening.asp / /

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