Difference between revisions of "McCune-Albright syndrome"

From Libre Pathology
Jump to navigation Jump to search
(create)
 
m
 
(3 intermediate revisions by the same user not shown)
Line 2: Line 2:


It is characterized by the triad:<ref>{{OMIM|174800}}</ref>
It is characterized by the triad:<ref>{{OMIM|174800}}</ref>
*Café-au-lait spots.
#Café-au-lait spots - unilateral.
*Polystotic [[fibrous dysplasia]].
#Polystotic [[fibrous dysplasia]].
*Precocious puberty.
#Precocious puberty.
 
Note:
*''Polyostotic'' = several bones involved.
 
==See also==
*[[Neurofibromatosis type 1]].


==References==
==References==

Latest revision as of 07:37, 13 January 2012

McCune-Albright syndrome is a genetic disorder.

It is characterized by the triad:[1]

  1. Café-au-lait spots - unilateral.
  2. Polystotic fibrous dysplasia.
  3. Precocious puberty.

Note:

  • Polyostotic = several bones involved.

See also

References

  1. ↑ Online 'Mendelian Inheritance in Man' (OMIM) 174800
Retrieved from "https://librepathology.org/w/index.php?title=McCune-Albright_syndrome&oldid=11605"