Open main menu
Home
Random
Recent changes
Special pages
Community portal
Preferences
About Wikipedia
Disclaimers
Incubator escapee wiki
Search
User menu
Talk
Dark mode
Contributions
Create account
Log in
Editing
Primary familial brain calcification
(section)
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
{{short description|Genetic disorder involving calcification of the basal ganglia}} {{Infobox medical condition (new) | name = Primary familial brain calcification | synonyms = Familial idiopathic basal ganglia calcification | image = Fahr_syndrome.gif | caption = [[CT scan]] of characteristic calcifications of the disease | pronounce = | field = | symptoms = | complications = | onset = | duration = | types = | causes = | risks = | diagnosis = | differential = | prevention = | treatment = | medication = | prognosis = | frequency = | deaths = }} '''Primary familial brain calcification'''<ref name=ncbi>{{cite journal|url=https://www.ncbi.nlm.nih.gov/books/NBK1421/|title=Primary Familial Brain Calcification|author1=Eliana Marisa Ramos | author2=Joao Oliveira | author3=Maria J Sobrido | author4= Giovanni Coppola|website=GeneReviews, at [[National Center for Biotechnology Information]]|publisher=University of Washington, Seattle|year=1993|pmid=20301594 }} Initial Posting: April 18, 2004; Last Update: August 24, 2017.</ref> (PFBC), also known as '''familial idiopathic basal ganglia calcification''' ('''FIBGC''') and '''Fahr's disease''',<ref name=ncbi/> is a rare,<ref>{{cite web |url=http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&diseaseID=8272 |title=Genetic and Rare Diseases Information Center (GARD) β an NCATS Program | Providing information about rare or genetic diseases |access-date=2009-06-13 |url-status=dead |archive-url=https://web.archive.org/web/20090511075059/http://rarediseases.info.nih.gov/GARD/Disease.aspx?PageID=4&DiseaseID=8272 |archive-date=2009-05-11 }}</ref> [[Dominance_(genetics)|genetically dominant or recessive]], inherited [[neurology|neurological]] disorder characterized by abnormal deposits of [[calcium]] in areas of the [[brain]] that control movement. Through the use of [[Computed tomography|CT scans]], calcifications are seen primarily in the [[basal ganglia]] and in other areas such as the [[cerebral cortex]].<ref>{{cite journal |author1=Benke T | author2= Karner E | author3=Seppi K| author4=Delazer M | author5=Marksteiner J | author6=Donnemiller E |title=Subacute dementia and imaging correlates in a case of Fahr's disease |journal=J. Neurol. Neurosurg. Psychiatry |volume=75 |issue=8 |pages=1163β5 |date=August 2004 |pmid=15258221 |pmc=1739167 |doi=10.1136/jnnp.2003.019547 |url=}}</ref>
Edit summary
(Briefly describe your changes)
By publishing changes, you agree to the
Terms of Use
, and you irrevocably agree to release your contribution under the
CC BY-SA 4.0 License
and the
GFDL
. You agree that a hyperlink or URL is sufficient attribution under the Creative Commons license.
Cancel
Editing help
(opens in new window)