Galactokinase Deficiency
This is one of several disorders of metabolism in galactose (sugar molecule found in many foods) which is not utilized properly as the result of a defective enzyme.
Alternate Names : Galactose-1-phosphate uridyl transferase deficiency, Galactokinase deficiency, Galactose-6-phosphate epimerase deficiency
Definition ...
Galactokinase deficiency
Uridine diphosphate galactose 4-epimerase deficiency
Diagnosis ...
Galactokinase deficiency
Galactorrhea-Amenorrhea Syndrome
Galactorrhea-Amenorrhea without Pregnancy
Galactose-1-Phosphate Uridyl Transferase Deficiency
Galactose-6-phosphatase emirase deficiency
Galactosemia
Galactosemia - Support Group ...
Galactokinase deficiency
Galactose-1-phosphate uridyl transferase deficiency
Galactose-6-phosphate epimerase deficiency
Galactosemia
Galactosylceramidase deficiency
Galactosylcerebrosidase deficiency
Gallbladder attack
Gallbladder disease ...
type V, type VI, type VII) - fructose metabolism (Fructose intolerance, Fructose bisphosphatase deficiency, Essential fructosuria) - galactose metabolism (Galactosemia, Galactose-1-phosphate uridylyltransferase galactosemia, Galactokinase deficiency) ...
nervous system, Diverticulosis, Esophageal, Early Mobilizations, Earth, Infusorial, Enamel Permeability, Dental, Erythroid Colony-Forming Unit, Ethylsuccinate, Erythromycin, Fever Blisters, Folyl Conjugate Synthetase, Galactokinase Deficiency ...
A less severe form of this disease is due to galactokinase deficiency. This type may be managed with a few dietary restrictions. It does not carry the risk of neurologic or liver damage.
Galactose-1-phosphate uridyl transferase deficiency; Galactokinase deficiency; Galactose-6-phosphate epimerase deficiency
Causes
Galactosemia is an inherited disorder. This means it is passed down through families.
 See also: Galactosemia, Deficiency, Pregnancy, Glycogen Storage Disease, Storage disease
  
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