Megacystis microcolon intestinal hypoperistalsis syndrome
Other Names for this Disease
- MMIH syndrome
- Berdon syndrome
- Megacystis-microcolon-intestinal hypoperistalsis syndrome
- Megacystis-microcolon-intestinal hypoperistalsis-hydronephrosis syndrome
This condition is part of a group of disorders caused by mutations in the ACTG2 gene. ACTG2-related disorders are inherited in an autosomal dominant manner.
Last updated: 8/19/2015
- Wangler MF. ACTG2-Related Disorders. GeneReviews. June 11, 2015; http://www.ncbi.nlm.nih.gov/books/NBK299311/. Accessed 8/19/2015.