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Differential Diagnosis For Ataxia: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Hypoglycemia, reactive diabetic
Nocturnal hypoglycemia/insulin
Diabetic amyotrophy syndrome
Diabetic peripheral neuropathy
Primary lactic acidemia/children
Kernicterus
Abetalipoproteinemia (Bassen Kornzweig)
Combined carboxylase/Biotinidase deficiency
French-Canadian type COX mitochondrial defect
Mitochondrial respiratory chain defects
Pyruvate carboxylase enzyme deficiency/PCD
Pyruvate Dehydrogenase Complex Deficiency/PDCD
Infantile mitochondrial myopathy/Cox defect
Cerebral lipidosis disorder
Ornithine Transcarbamylase (OTC) defic.
Sialidosis/Cherry Red Spot Myoclonus
Wilsons Disease
Adult ceroid lipofuscinosis/Kufs
Gangliosidosis, generalized (GM1)
Hartnup disease
Infantile ceroid lipofuscinosis/Finnish (Santvuori-Haltia)
Juvenile ceroid lipofuscinosis/Batten-M
Maple syrup urine disease
Niemann-Pick disease
Sandhoff disease
Sanfilippo's mucopolysaccharidosis synd
Tryptophanemia
Urea cycle/metabolic disorder
Goldberg Syndrome
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