Related Conditions & Treatments | Boston Children's Hospital

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Conditions & Treatments

Condition

DGAT-1 Deficiency

DGAT-1 deficiency is a rare genetic disease that causes diarrhea, inability to absorb nutrients, and poor growth.

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Condition

Glucose Galactose Malabsorption

Glucose galactose malabsorption is when a child’s body cannot absorb the simple sugars glucose and galactose.

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Condition

Microvillus Inclusion Disease

Microvillus inclusion disease (MVID) is a rare genetic disease of the intestine that causes severe diarrhea and an inability to absorb nutrients.

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Condition

Trichohepatoenteric Syndrome

Trichohepatoenteric syndrome is an extremely rare genetic condition that affects a child’s hair, liver, and intestines.

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Condition

TTC7A Deficiency

TTC7A deficiency is a rare genetic disease that causes diarrhea, inflammation of the intestines, bowel obstructions, immune dysfunction, and an inability to absorb nutrients.

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Condition

Tufting Enteropathy

Tufting enteropathy is a rare genetic disease of the intestine that causes severe diarrhea and an inability to absorb nutrients.

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Contact the Congenital Enteropathy Program 617-355-7368

International +1-617-355-5209

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Conditions & Treatments

DGAT-1 Deficiency

Glucose Galactose Malabsorption

Microvillus Inclusion Disease

Trichohepatoenteric Syndrome

TTC7A Deficiency

Tufting Enteropathy

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