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Alactasia, hereditary (medical condition): A congenital metabolic disorder where a deficiency of an enzyme called...more »
See also:
Congenital lactase deficiency:
»Introduction: Congenital lactase deficiency
»Symptoms of Congenital lactase deficiency
»Treatments for Congenital lactase deficiency
Alactasia, hereditary: The condition resulting from the absence or deficiency of LACTASE in the MUCOSA cells of the GASTROINTESTINAL TRACT, and the inability to break down LACTOSE in milk for ABSORPTION. Bacterial fermentation of the unabsorbed lactose leads to symptoms that range from a mild indigestion (DYSPEPSIA) to severe DIARRHEA. Lactose intolerance may be an inborn error or acquired.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Alactasia, hereditary:
Alactasia, hereditary: Another name for Congenital lactase deficiency (or close medical condition association).
»Introduction: Congenital lactase deficiency
»Symptoms of Congenital lactase deficiency
»Treatments for Congenital lactase deficiency
Alactasia, hereditary: Alactasia, hereditary is listed as a type of (or associated with) the following medical conditions in our database:
Some of the symptoms of Alactasia, hereditary incude:
See full list of 13 symptoms of Alactasia, hereditary (Congenital lactase deficiency)
Treatments for Alactasia, hereditary (Congenital lactase deficiency) include:
Read more about treatments for Alactasia, hereditary
Treatment of Alactasia, hereditary: For more treatment information about Alactasia, hereditary, see treatment of Congenital lactase deficiency (Alactasia, hereditary)
Source: Diseases Database
Source: Diseases Database
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