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Differential Diagnosis For Nocturnal awakenings Events Phenomenon, Newborn screening tests abnormal (extended): Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Biochemical Causes
Diabetic autonomic neuropathy syndrome
Nocturnal hypoglycemia/insulin
Diabetic peripheral neuropathy
Polyneuropathy, diabetic
Diabetic diarrhea syndrome
Carnitine/Acylcarnitine translocase deficiency
Citrullinemia/Argininsuccinicaciduria
HyperArgininemia
Ketotic hyperglycinemia, idiopathic
Methyl crotonyl CoA carboxylase deficiency
Methylmalonic acidemia/ketotic glycine
Phenylketonuria/PKU
Propionicacidemia/ketotic glycinemia
Pyroglutamic acidemia
Acyl-CoA Dehydrogenase/short chain def
Aminoacid enzyme/metabolic disorder
Hyperammonemia, hereditary
LCHAD/Long chain OH-CoA dehydrogenase def
MCAD/Medium chain OH-CoA Dehydrogenase def
Ornithine Transcarbamylase (OTC) defic.
Ornithinemia
Proprionic acidemia/congenital
Tyrosinemia, hereditary
VLCHAD/Very Long chain OH-CoA dehydrogenase def
Aminoaciduria
Carnitine palmityltranferase deficiency
Citrullinuria
Glutaric aciduria/Acidemia
Homocystinuria/homocystinemia
Maple syrup urine disease
Tetrahydrobiopterin deficiency/Atypical PKU
Urea cycle/metabolic disorder
Fatty acid oxidation/metabolic syndromes
Hyperammonemia/Ornithemia/Homocitrullinuris/HHH
Organic acidemias/Metabolic syndromes
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