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Differential Diagnosis For Seizures: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Nocturnal hypoglycemia/insulin
Metabolic disorders
Methemoglobinemia, Hereditary
Porphyria variegata
Porphyria, acute intermittent
Kernicterus
Tay-Sachs disease
Combined carboxylase/Biotinidase deficiency
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
HyperArgininemia
Phenylketonuria/PKU
Pyruvate carboxylase enzyme deficiency/PCD
Infantile mitochondrial myopathy/Cox defect
Pyridoxine dependency
Aminoacid enzyme/metabolic disorder
Beta-alaninemia
Cerebral lipidosis disorder
Hyperglycinemia, nonketotic
Prolinemia/type II
Sialidosis/Cherry Red Spot Myoclonus
Succinic Semialdehyde dehydrogenase Deficiency
Wilsons Disease
Adult ceroid lipofuscinosis/Kufs
Alpha-NAGA deficency (Schindler)
Beta-glucuronidase deficiency syndrome (MPS VII)
Coproporphyria, hereditary
Fructose intolerance, hereditary
Fucosidosis (Anderson-Fabry)
Galactosemia
Gangliosidosis, generalized (GM1)
Glycogen storage diseases
Homocystinuria/homocystinemia
Infantile ceroid lipofuscinosis/Finnish (Santvuori-Haltia)
Maple syrup urine disease
McArdle's syndrome
Sandhoff disease
Tetrahydrobiopterin deficiency/Atypical PKU
Von Gierke's disease/glycogenosis I
Goldberg Syndrome
Methemoglobinemia, acquired/toxic
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