Microvillous inclusion disease

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Microvillous inclusion disease
Synonyms	Microvillus inclusion disease, Davidson's disease
Pronounce	N/A
Specialty	N/A
Symptoms	Severe chronic diarrhea, dehydration, malnutrition
Complications	N/A
Onset	Neonatal period
Duration	Lifelong
Types	N/A
Causes	Mutations in the MYO5B gene
Risks	Consanguinity
Diagnosis	Electron microscopy of intestinal biopsy, genetic testing
Differential diagnosis	Congenital chloride diarrhea, congenital sodium diarrhea, tufting enteropathy
Prevention	N/A
Treatment	Total parenteral nutrition, intestinal transplantation
Medication	N/A
Prognosis	Poor without treatment
Frequency	Rare
Deaths	N/A

Microvillous inclusion disease (MVID) is a rare congenital disorder that affects the intestines, leading to severe, chronic diarrhea and malabsorption. It is also known as congenital microvillus atrophy. The disease is typically diagnosed in infancy and can be life-threatening if not managed properly.

Pathophysiology

MVID is characterized by the presence of microvillus inclusions within the epithelial cells of the small intestine. These inclusions are abnormal structures that result from the improper formation and function of microvilli, which are tiny, finger-like projections on the surface of epithelial cells that increase the surface area for absorption. The defective microvilli lead to impaired nutrient absorption and chronic diarrhea.

Genetics

The disease is usually inherited in an autosomal recessive manner. Mutations in the MYO5B gene, which encodes the protein myosin Vb, are commonly associated with MVID. This protein is crucial for the proper trafficking of vesicles within cells, and its dysfunction leads to the formation of microvillus inclusions.

Clinical Presentation

Infants with MVID typically present with severe, watery diarrhea shortly after birth. Other symptoms may include:

• Failure to thrive
• Dehydration
• Electrolyte imbalances
• Malnutrition

Diagnosis

Diagnosis of MVID is based on clinical presentation, histological examination of intestinal biopsies, and genetic testing. The presence of microvillus inclusions in enterocytes observed under an electron microscope is a key diagnostic feature.

Treatment

There is no cure for MVID, and treatment focuses on managing symptoms and complications. This may include:

• Total parenteral nutrition (TPN) to provide essential nutrients intravenously
• Management of dehydration and electrolyte imbalances
• Potential small bowel transplantation in severe cases

Prognosis

The prognosis for individuals with MVID varies. With appropriate management, some patients can achieve a relatively stable condition, but the disease can be life-threatening, especially in cases where complications arise or treatment is not adequately managed.

See also

• Microvillus
• Autosomal recessive
• MYO5B
• Total parenteral nutrition
• Small bowel transplantation

See Also

• Congenital disorders of glycosylation
• Intestinal atresia
• Short bowel syndrome

External Links

-

This congenital disorder related article is a stub. You can help WikiMD by expanding it.

   This article is a medical stub. You can help WikiMD by expanding it!