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!
==History== The disease was first noted by [[Germany|German]] pathologist [[Karl Theodor Fahr]] in 1930.<ref>{{cite journal |author=Fahr, T. |title=Idiopathische Verkalkung der Hirngefässe |journal=Zentralblatt für Allgemeine Pathologie und Pathologische Anatomie |volume=50 |pages=129–133 |year=1930–1931 }} </ref><ref>{{WhoNamedIt|synd|451|Fahr's disease}}</ref> A less common name for the condition is Chavany-Brunhes syndrome and Fritsche's syndrome, the former named after Jacques Brunhes, [[Jean Alfred Émile Chavany]], while the later named after [[R. Fritsche]].<ref>{{WhoNamedIt|synd|1518|Chavany-Brunhes syndrome}}</ref><ref>{{Cite web |url=http://rarediseases.info.nih.gov/GARD/QnA.aspx?PageID=4&CaseID=22373&DiseaseID=8272 |title=Chavany-Brunhes syndrome |access-date=2009-06-13 |archive-date=2012-05-31 |archive-url=https://web.archive.org/web/20120531191623/http://rarediseases.info.nih.gov/GARD/QnA.aspx?PageID=4&CaseID=22373&DiseaseID=8272 |url-status=dead }}</ref> Fewer than 20 families had been reported in the literature up to 1997.<ref name=Kobari1997>{{cite journal |author1=Kobari M|author2=Nogawa S|author3=Sugimoto Y|author4=Fukuuchi Y |title=Familial idiopathic brain calcification with autosomal dominant inheritance |journal=Neurology |volume=48 |issue=3 |pages=645–9 |date=March 1997 |pmid=9065541 |doi=10.1212/wnl.48.3.645|s2cid=1061208 }}</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)