Hirschsprung's disease pathophysiology: Difference between revisions
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Hirschsprung’s disease is a [[congenital]] disorder of the colon in which certain nerve cells, known as ganglion cells, are absent, causing chronic constipation. <ref>Worman and Ganiats 1995, Am Fam Physician 51, 487-494 [http://www.ncbi.nlm.nih.gov/pubmed/7840044]</ref> | Hirschsprung’s disease is a [[congenital]] disorder of the colon in which certain nerve cells, known as ganglion cells, are absent, causing chronic constipation. <ref>Worman and Ganiats 1995, Am Fam Physician 51, 487-494 [http://www.ncbi.nlm.nih.gov/pubmed/7840044]</ref> | ||
==Pathophysiology== | ==Pathophysiology== | ||
==Genetic basis== | |||
In 2002, scientists thought they found the solution. According to this new research, the interaction between two proteins [[genetic code|encoded]] by two variant genes caused Hirschsprung’s. The [[RET proto-oncogene]] on [[chromosome 10]] was identified one of the [[gene]]s involved, and it was determined that [[mutation|dominant mutation]]s may occur within this [[gene]] leading to a loss of function for the protein it [[genetic code|encoded]] (Passarge 11). The protein with which RET has to interact in order for Hirschsprung’s disease to develop is termed EDNRB, and is encoded by the [[gene]] ''EDNRB'' located on [[chromosome 13 (human)|chromosome 13]]. Six other genes were discovered to be associated with Hirschsprung’s. According to the study, these genes are GDNF on [[chromosome 5 (human)|chromosome 5]], EDN3 on [[chromosome 20 (human)|chromosome 20]], SOX10 on [[chromosome 22 (human)|chromosome 22]], ECE1 on [[chromosome 1 (human)|chromosome 1]], NTN on [[chromosome 19 (human)|chromosome 19]], and SIP1 on [[chromosome 2 (human)|chromosome 2]]. These scientists concluded that the mode of inheritance for Hirschsprung’s is oligogenic inheritance (Passarge 11). This means that two mutated genes interact to cause a disorder. Variations in RET and EDNRB have to coexist in order for a child to get Hirschsprung’s. However, although six other genes were shown to have an effect on Hirschsprung’s, the researchers were unable to determine how they interacted with RET and EDNRB. Thus, the specifics of the origins of the disease are still not completely known. More recently, syndromic cases of Hischprung's disease (that is, associated with other defects of the [[autonomic nervous system]]) were shown to be caused by mutations in the homeobox gene [[PHOX2B]]. | |||
RET codes for proteins that help the neural crest cells (which become ganglion cells) move through the digestive tract during the development of the embryo (Sawin). EDNRB codes for proteins to actually connect these nerve cells to the digestive tract. This means that the absence of certain nerve fibers in the colon could be directly related to these two genes mutating so the wrong proteins are produced. Research published in June of 2004 suggests that there are actually ten genes associated with Hirschsprung’s disease (Puri and Shinkai). Also, new research suggests that mutations in genomic sequences involved in regulating EDNRB have a bigger impact on Hirschsprung’s disease than previously thought. | |||
Dr. Bob Sawin of Seattle’s Children's Hospital notes that it is generally accepted in the scientific community that the gene RET is the most important gene when looking for the genetic cause of Hirschsprung’s disease. RET can mutate in many ways, and is associated with Down syndrome. Since [[Down Syndrome]] is comorbid in two percent of Hirschsprung’s cases, there is a likelihood that RET is involved heavily in both Hirschprung's disease and Down Syndrome. RET is also associated with [[thyroid cancer]] and [[neuroblastoma]] (Sawin). Both of these disorders have also been observed in Hirschsprung’s patients with greater frequency than in the general population. One function that RET controls is the travel of the [[neural crest cell]]s through the [[intestine]]s in the developing [[fetus]]. When RET mutations cause Hirschsprung’s disease, “the cells start traveling through the colon, only to be stopped once the mutation occurs” (Sawin). The earlier the mutation of RET occurs in Hirschsprung’s disease, the more severe the disorder becomes (Sawin). | |||
While researchers remain uncertain of the exact genetic cause of Hirschsprung’s disease, Dr. Sawin notes that in familial cases, (in which families have multiple affected patients) Hirschsprung’s disease exhibits autosomal dominant transmission, with the gene RET being dominant. However, in sporadic cases, Sawin notes that there has been no inheritance pattern identified. | |||
Treating Hirschsprung’s is much easier than determining the genetic causes of this disorder. The only way to treat Hirschsprung’s disease is through surgery (National Digestive Diseases Information Clearinghouse). If Hirschsprung’s goes untreated, the patient can develop [[enterocolitis]], the inflammation of the small intestine and the colon (Sawin). This was the cause of death of the two boys that Harald Hirschsprung observed. Surgery is now used to remove the non-functioning portion of the bowel in order to restore bowel function (Sawin). | |||
Hirschsprung's disease, hypoganglionosis, gut dysmotility, gut transit disorders and intussusception have been recorded with the dominantly inherited neurovisceral porphyrias (acute intermittent porphyria, hereditary coproporphyria, variegate porphyria). Children may require enzyme or DNA testing for these disorders as they may not produce or excrete porphyrins prepuberty. | |||
===Video: Histopathological Findings === | ===Video: Histopathological Findings === | ||
Revision as of 16:20, 19 March 2013
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Overview
Hirschsprung’s disease is a congenital disorder of the colon in which certain nerve cells, known as ganglion cells, are absent, causing chronic constipation. [1]
Pathophysiology
Genetic basis
In 2002, scientists thought they found the solution. According to this new research, the interaction between two proteins encoded by two variant genes caused Hirschsprung’s. The RET proto-oncogene on chromosome 10 was identified one of the genes involved, and it was determined that dominant mutations may occur within this gene leading to a loss of function for the protein it encoded (Passarge 11). The protein with which RET has to interact in order for Hirschsprung’s disease to develop is termed EDNRB, and is encoded by the gene EDNRB located on chromosome 13. Six other genes were discovered to be associated with Hirschsprung’s. According to the study, these genes are GDNF on chromosome 5, EDN3 on chromosome 20, SOX10 on chromosome 22, ECE1 on chromosome 1, NTN on chromosome 19, and SIP1 on chromosome 2. These scientists concluded that the mode of inheritance for Hirschsprung’s is oligogenic inheritance (Passarge 11). This means that two mutated genes interact to cause a disorder. Variations in RET and EDNRB have to coexist in order for a child to get Hirschsprung’s. However, although six other genes were shown to have an effect on Hirschsprung’s, the researchers were unable to determine how they interacted with RET and EDNRB. Thus, the specifics of the origins of the disease are still not completely known. More recently, syndromic cases of Hischprung's disease (that is, associated with other defects of the autonomic nervous system) were shown to be caused by mutations in the homeobox gene PHOX2B.
RET codes for proteins that help the neural crest cells (which become ganglion cells) move through the digestive tract during the development of the embryo (Sawin). EDNRB codes for proteins to actually connect these nerve cells to the digestive tract. This means that the absence of certain nerve fibers in the colon could be directly related to these two genes mutating so the wrong proteins are produced. Research published in June of 2004 suggests that there are actually ten genes associated with Hirschsprung’s disease (Puri and Shinkai). Also, new research suggests that mutations in genomic sequences involved in regulating EDNRB have a bigger impact on Hirschsprung’s disease than previously thought.
Dr. Bob Sawin of Seattle’s Children's Hospital notes that it is generally accepted in the scientific community that the gene RET is the most important gene when looking for the genetic cause of Hirschsprung’s disease. RET can mutate in many ways, and is associated with Down syndrome. Since Down Syndrome is comorbid in two percent of Hirschsprung’s cases, there is a likelihood that RET is involved heavily in both Hirschprung's disease and Down Syndrome. RET is also associated with thyroid cancer and neuroblastoma (Sawin). Both of these disorders have also been observed in Hirschsprung’s patients with greater frequency than in the general population. One function that RET controls is the travel of the neural crest cells through the intestines in the developing fetus. When RET mutations cause Hirschsprung’s disease, “the cells start traveling through the colon, only to be stopped once the mutation occurs” (Sawin). The earlier the mutation of RET occurs in Hirschsprung’s disease, the more severe the disorder becomes (Sawin).
While researchers remain uncertain of the exact genetic cause of Hirschsprung’s disease, Dr. Sawin notes that in familial cases, (in which families have multiple affected patients) Hirschsprung’s disease exhibits autosomal dominant transmission, with the gene RET being dominant. However, in sporadic cases, Sawin notes that there has been no inheritance pattern identified.
Treating Hirschsprung’s is much easier than determining the genetic causes of this disorder. The only way to treat Hirschsprung’s disease is through surgery (National Digestive Diseases Information Clearinghouse). If Hirschsprung’s goes untreated, the patient can develop enterocolitis, the inflammation of the small intestine and the colon (Sawin). This was the cause of death of the two boys that Harald Hirschsprung observed. Surgery is now used to remove the non-functioning portion of the bowel in order to restore bowel function (Sawin).
Hirschsprung's disease, hypoganglionosis, gut dysmotility, gut transit disorders and intussusception have been recorded with the dominantly inherited neurovisceral porphyrias (acute intermittent porphyria, hereditary coproporphyria, variegate porphyria). Children may require enzyme or DNA testing for these disorders as they may not produce or excrete porphyrins prepuberty.
Video: Histopathological Findings
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