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Differential Diagnosis For Failure to Thrive Child: Metabolic, Storage Disorders

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List of current finding(s):

Metabolic, Storage Disorders: next: Deficiency Causes
Diabetes mellitus, poorly controlled
Diabetes mellitus
Renal tubular disorders/metabolic
Diabetes mellitus/juvenile (Type I)
Kernicterus
Renal tubular acidosis type IV
Xanthinuria
Newborn diabetes mellitus, transient
Methylmalonic acidemia/ketotic glycine
Acyl-CoA Dehydrogenase/short chain def
Aminoacid enzyme/metabolic disorder
LCHAD/Long chain OH-CoA dehydrogenase def
MCAD/Medium chain OH-CoA Dehydrogenase def
Tyrosinemia, hereditary
VLCHAD/Very Long chain OH-CoA dehydrogenase def
Wolman Disease
Aminoaciduria
Carnitine deficiency syndrome
Farber disease/ceramide lipidosis
Fructose intolerance, hereditary
Fucosidosis (Anderson-Fabry)
Galactosemia
Gangliosidosis, generalized (GM1)
Glycogen storage diseases
Hartnup disease
Maple syrup urine disease
Niemann-Pick disease
Phosphoenolpyruvate carboxykinase defic (PEPCK)
Storage (storage-cell) disorders
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