Microvillus inclusion disease (MVID) is a rare genetic disease of the intestine that causes severe diarrhea and an inability to absorb nutrients. It usually starts soon after birth and is one of a …

Microvillus inclusion disease usually occurs days or hours after birth, in the form of malabsorption. Learn about the symptoms, diagnosis, and treatment.

Microvillus inclusion disease is caused by genetic mutations, also known as pathogenic variants. Genetic mutations can be hereditary, when parents pass them down to their children, or they …

Microvillus inclusion disease has an autosomal recessive pattern of inheritance.

Microvillus inclusion disease (MVID) is a very rare and severe intestinal disease characterized by intractable neonatal secretory diarrhea persisting at bowel rest and specific histological …

Nov 17, 2022 · Learn about Microvillus Inclusion Disease, including symptoms, causes, and treatments. If you or a loved one is affected by this condition, visit NORD to find.

Microvillus Inclusion Disease (MVID) is a rare disease of the digestive tract characterized by an alteration of the microvilli of the small intestine, resulting in profuse and intractable watery …

Microvillus inclusion disease (MVID; OMIM 251850) is a rare autosomal recessive disease presenting with severe intractable diarrhea and malabsorption in neonates. An early onset and …

Sep 25, 2025 · MVID is caused by a mutation in the Myo5b gene and follows an autosomal recessive inheritance pattern. The Myo5b gene regulates proteins in the epithelial lining of the …

Feb 22, 2024 · Microvillus inclusion disease (MVID) is a rare type of congenital enteropathy in infants that causes devastating diarrhea and an inability to absorb food. Infants can lose liters …