A case report of a 30-year-old male with megacystis-microcolon-intestinal hypoperistalsis syndrome with de novo ACTG2 gene mutation
Introduction: Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS) is a very rare genetic disorder of visceral motility of the gastrointestinal and genitourinary system. According to our knowledge, so far there has been no description of a patient with megacystis-microcolon-intestinal h...
Saved in:
Main Authors: | Knežević Violeta V. (Author), Knežević Aleksandar D. (Author), Milijašević Dragana S. (Author), Božić Dušan Đ. (Author), Milijašević Boris Ž. (Author) |
---|---|
Format: | Book |
Published: |
Srpsko lekarsko drustvo,
2023-01-01T00:00:00Z.
|
Subjects: | |
Online Access: | Connect to this object online. |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Megacystis-Microcolon-intestinal hypoperistalsis syndrome
by: Ahmed Elrouby, et al.
Published: (2019) -
Megacystis microcolon intestinal hypoperistalsis syndrome complicated by perforation
by: Jain Vishal, et al.
Published: (2011) -
Megacystis Microcolon Intestinal Hypoperistalsis Syndrome (MMIHS): A Rarity
by: Naeem Liaqat, et al.
Published: (2015) -
Megacystis microcolon intestinal hypoperistalsis syndrome overlapping prune belly syndrome
by: Hidehiko Maruyama, et al.
Published: (2018) -
Syndromic and single gene disorders associated with fetal megacystis (I): Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIHS)
by: Chih-Ping Chen
Published: (2024)