Genetic Brain Disorders Update [LIBRARY OF GENETIC BRAIN DISORDERS ► NEW TOPIC PAGE]

Genetic Brain Disorders Update

Genetic Brain Disorders Update

MedlinePlus sent this bulletin at 04/14/2016 01:10 PM EDT

New on the MedlinePlus Genetic Brain Disorders page:

Genetics Home Reference: glutaric acidemia type I

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: phosphoglycerate kinase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glutamate formiminotransferase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: propionic acidemia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: phosphoglycerate dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: leukoencephalopathy with brainstem and spinal cord involvement and lactate elevation

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: molybdenum cofactor deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: prion disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: fucosidosis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: succinic semialdehyde dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mitochondrial neurogastrointestinal encephalopathy disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: prolidase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: moyamoya disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: fumarase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: galactosemia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mitochondrial complex III deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: myoclonic epilepsy with ragged-red fibers

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: malonyl-CoA decarboxylase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: pyruvate carboxylase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: hyperprolinemia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glycine encephalopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mucopolysaccharidosis type III

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glutathione synthetase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: phosphoribosylpyrophosphate synthetase superactivity

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mucopolysaccharidosis type II

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: holocarboxylase synthetase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: pyruvate dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mucopolysaccharidosis type I

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: hypermethioninemia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: mucolipidosis type IV

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: maple syrup urine disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: ethylmalonic encephalopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: ornithine translocase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: fragile X-associated tremor/ataxia syndrome

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: ornithine transcarbamylase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: guanidinoacetate methyltransferase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: isovaleric acidemia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: multiple sulfatase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: sialic acid storage disease

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: dentatorubral-pallidoluysian atrophy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: alpha-methylacyl-CoA racemase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: ataxia neuropathy spectrum

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: biotinidase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: alpha-mannosidosis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: aspartylglucosaminuria

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: adenylosuccinate lyase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: arginase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: carbamoyl phosphate synthetase I deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: arginine:glycine amidinotransferase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: argininosuccinic aciduria

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: cerebrotendinous xanthomatosis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: deoxyguanosine kinase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: beta-ketothiolase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: dihydropyrimidine dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: beta-mannosidosis

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: aromatic l-amino acid decarboxylase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: dihydrolipoamide dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: childhood myocerebrohepatopathy spectrum

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: citrullinemia

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: aminoacylase 1 deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: combined malonic and methylmalonic aciduria

04/13/2016 02:39 PM EDT

Source: National Library of Medicine -