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Differential Diagnosis For Hyperhidrosis/Chronic sweating excess, Neonatal metabolic screening (mass spec) abnormal: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Hypoglycemia, reactive diabetic
Obesity, massive
Diabetic autonomic neuropathy syndrome
Nocturnal hypoglycemia/insulin
Obesity
Porphyria variegata
Porphyria, acute intermittent
2,4 Dienoyl-CoA reductase deficiency
Carnitine/Acylcarnitine translocase deficiency
Citrullinemia/Argininsuccinicaciduria
Combined carboxylase/Biotinidase deficiency
Hydroxybutyric acidemia
Hydroxymethylglutaryl CoA lyase deficiency
HyperArgininemia
Isobutyryl-CoA dehydrogenase deficiency
Ketothiolase deficiency
Ketotic hyperglycinemia, idiopathic
Methyl crotonyl CoA carboxylase deficiency
Methylmalonic acidemia/ketotic glycine
Phenylketonuria/PKU
Propionicacidemia/ketotic glycinemia
Pyroglutamic acidemia
Trifunctional protein deficiency/metabolic
Acyl-CoA Dehydrogenase/short chain def
Beta-hydroxyisolvaleric acidemia
LCHAD/Long chain OH-CoA dehydrogenase def
MCAD/Medium chain OH-CoA Dehydrogenase def
Proprionic acidemia/congenital
Tyrosinemia, hereditary
VLCHAD/Very Long chain OH-CoA dehydrogenase def
Carnitine palmityltranferase deficiency
Fucosidosis (Anderson-Fabry)
Galactosemia
Glutaric aciduria/Acidemia
Glutaric aciduria/type II
Homocystinuria/homocystinemia
Maple syrup urine disease
Pipecolic acidemia
Hyperammonemia/Ornithemia/Homocitrullinuris/HHH
Hypermethioninemia
Organic acidemias/Metabolic syndromes
Unclassified fatty oxidation syndromes (U-FAOD)
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