Web16 jul. 2024 · Disease Overview Mowat-Wilson syndrome (MWS) is a rare genetic disorder that may be apparent at birth or later in childhood. MWS is characterized by intellectual disability, distinctive facial features and seizures. WebLa malattia di Hirschsprung (HSCR), o megacolon congenito agangliare, è una malattia congenita dell' intestino caratterizzata dall'assenza, per un tratto del canale alimentare, del plesso mioenterico e del plesso sottomucoso, che garantiscono la coordinazione dei movimenti peristaltici intestinali. [1] [2]
Aganglionic megacolon - NIH Genetic Testing Registry (GTR) - NCBI
Web23 sep. 2024 · Hirschsprung disease can cause constipation, diarrhea, and vomiting. Sometimes it leads to serious colon problems, like enterocolitis and toxic megacolon, which can be life-threatening. So it's … Web12. De la Torre-Mondragón L, Ortega-Salgado JA. Transanalendorectal pull-through for Hirschsprung's disease. J Pediatr Surg. 1998;33:1283-6. [ Links ] 13. So HB, Schwartz DL, Becker JM, Daum F, Schneider KM. Endorectal pull-through without preliminary colostomy in neonates with Hirschsprung's disease. protogen ref sheet
Aganglionic megacolon (Concept Id: C0019569) - National Center …
WebHirschsprung disease (aganglionic megacolon) occurs when certain nerve cells in the wall of the colon do not form the right way when the fetus is growing. In a person who does not have Hirschsprung disease, large muscles move gas and stool through the colon with the help of nerve cells called ganglion cells. Web11 feb. 2024 · Congenital aganglionic megacolon, also called Hirschsprung disease, is … Web11 jun. 2024 · Hirschsprungs sygdom (HS) er en medfødt tilstand med manglende ganglieceller i den syge tarm, som forårsager manglende peristaltik og deraf følgende intestinal obstruktion 2. Fravær af ganglieceller medfører spasme i glat muskulatur i det afficerede tarmsegment og derved partiel eller total obstruktion. Sygdommen kaldes … resonance synthwave