A Novel Mutation in ACTG2 Gene in Mother with Chronic Intestinal Pseudoobstruction and Fetus with Megacystis Microcolon Intestinal Hypoperistalsis Syndrome

Background. A novel mutation in the ACTG2 gene is described in a pregnant patient followed up for chronic intestinal pseudoobstruction (CIPO) during pregnancy and her fetus with megacystis microcolon intestinal hypoperistalsis syndrome (MMIHS). Case. 24-year-old gravida 1 para 1 with CIPO and persis...

Descripción completa

Detalles Bibliográficos
Autores principales: Whittington, Julie R., Poole, Aaron T., Dutta, Eryn H., Munn, Mary B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745697/
https://www.ncbi.nlm.nih.gov/pubmed/29387497
http://dx.doi.org/10.1155/2017/9146507

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745697/
https://www.ncbi.nlm.nih.gov/pubmed/29387497
http://dx.doi.org/10.1155/2017/9146507

Ejemplares similares