Short answer · Medically reviewed summary · Last updated: 2023-07-13
Microvillus Inclusion Disease (MVID) is a rare genetic disorder that affects the functioning of the intestines. It is characterized by severe diarrhea, malabsorption, and failure to thrive in affected infants.
What is the prevalence of Microvillus Inclusion Disease?
Prevalence of Microvillus Inclusion Disease: how many people are affected worldwide, differences by sex and region, with sources.
Microvillus Inclusion Disease (MVID) is a rare genetic disorder that affects the functioning of the intestines. It is characterized by severe diarrhea, malabsorption, and failure to thrive in affected infants. MVID is an autosomal recessive disorder, meaning that both parents must carry a mutated gene for their child to be affected.
Due to its rarity, the prevalence of Microvillus Inclusion Disease is relatively low. Exact figures are challenging to determine as it is often underdiagnosed or misdiagnosed. However, studies estimate that MVID affects approximately 1 in every 50,000 to 100,000 live births worldwide.
Infants with MVID typically present with symptoms within the first few days or weeks of life. The chronic diarrhea associated with the condition can lead to dehydration, electrolyte imbalances, and nutrient deficiencies. Early diagnosis and appropriate management are crucial for the long-term health and survival of affected individuals.
While the prevalence of Microvillus Inclusion Disease is relatively low, it is essential for healthcare professionals to be aware of this condition to ensure timely diagnosis and appropriate interventions for affected infants.
