![Rare diseases / Phenylketonuria / Newborn screening / Urea cycle disorder / Hypermethioninemia / Maple syrup urine disease / Amino acid / Protein / Citrullinemia / Health / Medicine / Genetic genealogy Rare diseases / Phenylketonuria / Newborn screening / Urea cycle disorder / Hypermethioninemia / Maple syrup urine disease / Amino acid / Protein / Citrullinemia / Health / Medicine / Genetic genealogy](https://www.pdfsearch.io/img/54da03e249614fcf831886d68e0f961f.jpg)
| Document Date: 2006-10-30 12:08:43 Open Document File Size: 27,26 KBShare Result on Facebook
Facility FACMG University of Tennessee Genetic Center / / IndustryTerm pharmaceutical supplements / treatment of these disorders / / MedicalCondition moderate enzyme deficiency / mental retardation / several different disorders / seizures / toxic encephalopathy / coma / amino acid disorder / Citrullinemia / urea cycle disorder / common disorder / lethargy / Cystathione beta synthase deficiency / vomiting / Maple Syrup Urine Disorder / oculocutaneous tyrosinemia / Tyrosinemia / severe illness / disorder / PKU / autosomal recessive disorders / amino acid disorders / clinically more severe disorder / disorder homocystinuria / deficiency / phenylketonuria / illness / disorders / Homocystinuria / hepatorenal tyrosinemia / / MedicalTreatment adjunctive therapies / hemodialysis / surgery / / Organization Tennessee Genetic Center / FACMG University / University of Tennessee / / Person Karla J Matteson / / Position nutritionist / / ProvinceOrState Tennessee / / Technology diagnostic tests / /
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