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Differential Diagnosis For Neurodevelopmental disorders - Causes, Tender epigastric area/Tenderness: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Primary lactic acidemia/children
Glucose 6 PD deficiency
Tay-Sachs disease
Abetalipoproteinemia (Bassen Kornzweig)
Combined carboxylase/Biotinidase deficiency
Ketotic hyperglycinemia, idiopathic
Methylmalonic acidemia/ketotic glycine
Molybdenum cofactor deficency
Phenylketonuria/PKU
Propionicacidemia/ketotic glycinemia
Pyruvate carboxylase enzyme deficiency/PCD
Pyruvate Dehydrogenase Complex Deficiency/PDCD
Cerebral lipidosis disorder
Krebs cycle/EM cycle metabolic disorder
Sialidosis/Cherry Red Spot Myoclonus
Adult ceroid lipofuscinosis/Kufs
Fructose 1,6 diphosphatase deficiency
Fucosidosis (Anderson-Fabry)
Gangliosidosis, generalized (GM1)
Gaucher's disease
Glutaric aciduria/Acidemia
Homocystinuria/homocystinemia
Juvenile ceroid lipofuscinosis/Batten-M
McArdle's syndrome
Niemann-Pick disease
Sanfilippo's mucopolysaccharidosis synd
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