What is Hirschsprung's disease?
What is Hirschsprung's disease?
- Hirschsprung's disease: A rare condition where abnormalities in the bowel muscles prevent it from contracting normally and pushing the fecal matter through which results in obstruction and dilation of the bowel.
- Hirschsprung's disease: Congenital MEGACOLON resulting from the absence of ganglion cells (aganglionosis) in a distal segment of the LARGE INTESTINE. The aganglionic segment is permanently contracted thus causing dilatation proximal to it. In most cases, the aganglionic segment is within the RECTUM and SIGMOID COLON.
Source - Diseases Database
- Hirschsprung's disease: congenital condition in which the colon does not have the normal network of nerves; there is little urge to defecate so the feces accumulate and cause megacolon.
Source - WordNet 2.1
Hirschsprung's disease is listed as a "rare disease" by the Office of
Rare Diseases (ORD) of the National Institutes of Health
(NIH). This means that Hirschsprung's disease, or a subtype of Hirschsprung's disease,
affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)
Hirschsprung's disease: Introduction
Types of Hirschsprung's disease:
Types of Hirschsprung's disease:
Broader types of Hirschsprung's disease:
Who gets Hirschsprung's disease?
Patient Profile for Hirschsprung's disease: Usually in infants from birth, but sometimes no symptoms till teens or adulthood.
Profile for Hirschsprung's disease:
HD usually occurs in children.
(Source: excerpt from What I need to know about Hirschsprung's disease: NIDDK)
How serious is Hirschsprung's disease?
Complications of Hirschsprung's disease:
see complications of Hirschsprung's disease
What causes Hirschsprung's disease?
Causes of Hirschsprung's disease: see causes of Hirschsprung's disease
Cause of Hirschsprung's disease: Congenital absence of nerves in part of the colon, from unclear causes. Some cases are genetic but others are not.
Causes of Hirschsprung's disease:
HD develops before a child is born. Normally, nerve cells grow in the
baby's intestine soon after the baby begins to grow in the womb. These
nerve cells grow down from the top of the intestine all the way to the
anus. With HD, the nerve cells stop growing before they reach the end.
No one knows why the nerve cells stop growing. But we do know that it's
not the mother's fault. HD isn't caused by anything the mother did while
she was pregnant.
(Source: excerpt from What I need to know about Hirschsprung's disease: NIDDK)
Risk factors for Hirschsprung's disease:
see
risk factors for Hirschsprung's disease
What are the symptoms of Hirschsprung's disease?
Symptoms of Hirschsprung's disease:
see symptoms of Hirschsprung's disease
Complications of Hirschsprung's disease:
see complications of Hirschsprung's disease
Can anyone else get Hirschsprung's disease?
Inheritance:
see inheritance of Hirschsprung's disease
Hirschsprung's disease: Testing
Diagnostic testing: see tests for Hirschsprung's disease.
Misdiagnosis: see misdiagnosis and Hirschsprung's disease.
How is it treated?
Treatments for Hirschsprung's disease:
see treatments for Hirschsprung's disease
Research for Hirschsprung's disease:
see research for Hirschsprung's disease
Organs Affected by Hirschsprung's disease:
Organs and body systems related to Hirschsprung's disease include:
Name and Aliases of Hirschsprung's disease
Main name of condition: Hirschsprung's disease
Other names or spellings for Hirschsprung's disease:
HD, megacolon, aganglionic, HSCR, Hirschsprung disease 1, HSCR 1, Aganglionic megacolon, Hirschsprung disease type 1
Aganglionic megacolon
Source - Diseases Database
Hirschsprung's disease, Congenital megacolon
Source - WordNet 2.1
Aganglionic megacolon, HSCR, HSCR 1, Hirschsprung disease 1, Hirschsprung disease type 1, Huntington's chorea, Huntington's disease, Huntington disease
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)
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