This colon belonged to a 29-year-old man who had complained of constipation for most of his life. The condition he endured is known as congenital aganglionic megacolon, or Hirschsprung’s disease. It occurs when nerves to part of the colon fail to develop and making it difficult for waste to move to the rectum (aganglionic means “without nerve cells”). This man was a normal infant up to the age of 18 months, with the exception of a rather large abdomen, coupled with some irregularity of bowels and some constipation. His condition progressed, with the severity of the constipation increasing along with the size of his abdomen. By the age of 16 he would go up to a month at a time without any bowel movements. At 20 he was exhibited at a dime ...
AbstractObjectiveTo describe the case of an infant with Hirschsprung's disease presenting as total c...
none5siHirschsprung’s disease (HD) or “congenital megacolon” is a congenital developmental disorder ...
SummaryHirschsprung’s disease is a congenital motility disorder that is easily overlooked as a cause...
I do not intend to give an account of the changing philosophies concerning the aetiology and treatme...
Congenital aganglionic mega colon (Hirschsprung’s disease) is a motor disorder in the gut, due...
<p>Hirschsprung’s disease (congenital megacolon) is caused by the failed migration of colonic gangli...
Hirschsprung’s disease (HD), or congenital megacolon, is a disease characterized by the absence of g...
To describe the case of an infant with Hirschsprung's disease presenting as total colonic agangliono...
Hirschsprung's disease is characterized by absence of ganglion cells in submucosal and myenteric ple...
To describe the case of an infant with Hirschsprung's disease presenting as total colonic agangliono...
Hirschsprung's disease is characterized by absence of ganglion cells in submucosal and myenteric ple...
Hirschsprung disease is a disease that attacks the human digestive system, mainly in the large<br />...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
Background: Acquired Megacolon (AMC) is a condition involving persistent dilatation and lengthening ...
AbstractObjectiveTo describe the case of an infant with Hirschsprung's disease presenting as total c...
none5siHirschsprung’s disease (HD) or “congenital megacolon” is a congenital developmental disorder ...
SummaryHirschsprung’s disease is a congenital motility disorder that is easily overlooked as a cause...
I do not intend to give an account of the changing philosophies concerning the aetiology and treatme...
Congenital aganglionic mega colon (Hirschsprung’s disease) is a motor disorder in the gut, due...
<p>Hirschsprung’s disease (congenital megacolon) is caused by the failed migration of colonic gangli...
Hirschsprung’s disease (HD), or congenital megacolon, is a disease characterized by the absence of g...
To describe the case of an infant with Hirschsprung's disease presenting as total colonic agangliono...
Hirschsprung's disease is characterized by absence of ganglion cells in submucosal and myenteric ple...
To describe the case of an infant with Hirschsprung's disease presenting as total colonic agangliono...
Hirschsprung's disease is characterized by absence of ganglion cells in submucosal and myenteric ple...
Hirschsprung disease is a disease that attacks the human digestive system, mainly in the large<br />...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
Congenital intestinal aganglionosis, also called Hirschsprung disease (HD), is defined as the absenc...
Background: Acquired Megacolon (AMC) is a condition involving persistent dilatation and lengthening ...
AbstractObjectiveTo describe the case of an infant with Hirschsprung's disease presenting as total c...
none5siHirschsprung’s disease (HD) or “congenital megacolon” is a congenital developmental disorder ...
SummaryHirschsprung’s disease is a congenital motility disorder that is easily overlooked as a cause...