Difference between revisions of "Wilson's disease"
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'''Wilson disease's''' is a rare autosomal recessive genetic disease characterized by abnormal copper transportation. It presentation may be atypical. | |||
==General== | |||
Epidemiology: | |||
*Rare autosomal recessive - mutation in copper-transporting adenosine triphosphatase (ATPase) gene (ATP7B).<ref name=emedicine183456>[http://emedicine.medscape.com/article/183456-overview http://emedicine.medscape.com/article/183456-overview]</ref><ref name=omim606882>{{OMIM|606882}}</ref> | |||
**Heterozygote carrier rate approximately 1/100 persons.<ref name=emedicine183456/> | |||
*Young individuals - usually 12-23 years old. | |||
**May have late-onset (symptomatic when >40 years old).<ref name=pmid17433323>{{Cite journal | last1 = Ferenci | first1 = P. | last2 = Członkowska | first2 = A. | last3 = Merle | first3 = U. | last4 = Ferenc | first4 = S. | last5 = Gromadzka | first5 = G. | last6 = Yurdaydin | first6 = C. | last7 = Vogel | first7 = W. | last8 = Bruha | first8 = R. | last9 = Schmidt | first9 = HT. | title = Late-onset Wilson's disease. | journal = Gastroenterology | volume = 132 | issue = 4 | pages = 1294-8 | month = Apr | year = 2007 | doi = 10.1053/j.gastro.2007.02.057 | PMID = 17433323 }}</ref> | |||
Clinical: | |||
*Kayser-Fleischer rings --> on slit-lamp examination (green eyes). | |||
*May present to psychiatry or appear to be abusing EtOH. | |||
*Serum ceruloplasmin - lower than normal. | |||
Etiology: | |||
*Excess copper -- due to genetic defect. | |||
==Microscopic== | |||
Features: | |||
*Nothing specific - known as the great mimicker of liver pathology. | |||
*[[Steatosis of the liver|Steatosis]]. | |||
*Portal fibrosis. | |||
==Stains== | |||
*Copper staining positive - '''only 15% of cases'''. | |||
**Other stains: rhodinine (red/orange granules = positive), orecin. | |||
Notes: | |||
*Copper staining is a non-specific finding seen in many liver diseases; it is associated with impaired bile secretion.<ref name=pmid2464523>{{cite journal |author=Miyamura H, Nakanuma Y, Kono N |title=Survey of copper granules in liver biopsy specimens from various liver abnormalities other than Wilson's disease and biliary diseases |journal=Gastroenterol. Jpn. |volume=23 |issue=6 |pages=633–8 |year=1988 |month=December |pmid=2464523 |doi= |url=}}</ref> | |||
Image: | |||
*[http://openi.nlm.nih.gov/legacy/detailedresult.php?img=3375662_yjbm_85_2_249_g03&req=4 Orecin staining in Wilson's diseae (nih.gov)]. | |||
==Additional testing== | |||
*Mass spectrometry - determine portion of copper. | |||
==See also== | |||
*[[Medical liver disease]]. | |||
==References== | |||
{{Reflist|2}} | |||
==External links== | |||
*[https://www.lhsc.on.ca/lab/metals/req.htm Trace metals laboratory (lhsc.on.ca)]. | |||
[[Category:Medical liver disease]] | |||
Revision as of 12:13, 14 September 2015
Wilson disease's is a rare autosomal recessive genetic disease characterized by abnormal copper transportation. It presentation may be atypical.
General
Epidemiology:
- Rare autosomal recessive - mutation in copper-transporting adenosine triphosphatase (ATPase) gene (ATP7B).[1][2]
- Heterozygote carrier rate approximately 1/100 persons.[1]
- Young individuals - usually 12-23 years old.
- May have late-onset (symptomatic when >40 years old).[3]
Clinical:
- Kayser-Fleischer rings --> on slit-lamp examination (green eyes).
- May present to psychiatry or appear to be abusing EtOH.
- Serum ceruloplasmin - lower than normal.
Etiology:
- Excess copper -- due to genetic defect.
Microscopic
Features:
- Nothing specific - known as the great mimicker of liver pathology.
- Steatosis.
- Portal fibrosis.
Stains
- Copper staining positive - only 15% of cases.
- Other stains: rhodinine (red/orange granules = positive), orecin.
Notes:
- Copper staining is a non-specific finding seen in many liver diseases; it is associated with impaired bile secretion.[4]
Image:
Additional testing
- Mass spectrometry - determine portion of copper.
See also
References
- ↑ 1.0 1.1 http://emedicine.medscape.com/article/183456-overview
- ↑ Online 'Mendelian Inheritance in Man' (OMIM) 606882
- ↑ Ferenci, P.; Członkowska, A.; Merle, U.; Ferenc, S.; Gromadzka, G.; Yurdaydin, C.; Vogel, W.; Bruha, R. et al. (Apr 2007). "Late-onset Wilson's disease.". Gastroenterology 132 (4): 1294-8. doi:10.1053/j.gastro.2007.02.057. PMID 17433323.
- ↑ Miyamura H, Nakanuma Y, Kono N (December 1988). "Survey of copper granules in liver biopsy specimens from various liver abnormalities other than Wilson's disease and biliary diseases". Gastroenterol. Jpn. 23 (6): 633–8. PMID 2464523.