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Differential Diagnosis For Vomiting: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Diabetic ketoacidosis/coma
Diabetes mellitus
Diabetic autonomic neuropathy syndrome
Ketoacidosis, diabetic , treatment
Diabetes mellitus/juvenile (Type I)
Nephropathy, acute gouty/hyperuricemic
Metabolic disorders
Methemoglobinemia, Hereditary
Porphyria variegata
Porphyria, acute intermittent
Kernicterus
Coproporphyria erythrohepatica
Citrullinemia/Argininsuccinicaciduria
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
Methylmalonic acidemia/ketotic glycine
Phenylketonuria/PKU
Propionicacidemia/ketotic glycinemia
Pyroglutamic acidemia
Pyruvate carboxylase enzyme deficiency/PCD
Infantile mitochondrial myopathy/Cox defect
Acyl-CoA Dehydrogenase/short chain def
Aminoacid enzyme/metabolic disorder
Carbamoyl phosphate synthetase defic
Krebs cycle/EM cycle metabolic disorder
MCAD/Medium chain OH-CoA Dehydrogenase def
N-Acetylglutamate synthetase deficiency
Ornithine Transcarbamylase (OTC) defic.
Amyloidosis, hereditary, neuropathic
Fructose intolerance, hereditary
Galactosemia
Lysine intolerance
Urea cycle/metabolic disorder
Methemoglobinemia, acquired/toxic
Organic acidemias/Metabolic syndromes
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