Hashimoto-Pritzker syndrome: Difference between revisions
Jump to navigation
Jump to search
No edit summary |
No edit summary |
||
| Line 1: | Line 1: | ||
__NOTOC__ | |||
{{SI}} | {{SI}} | ||
{{CMG}} | {{CMG}} | ||
{{SK}} Congenital self-healing reticulohistiocytosis; Hashimoto-Pritzker disease | |||
==Overview== | ==Overview== | ||
''' | '''Hashimoto–Pritzker syndrome''' is a condition that is a self-limited form of [[Langerhans cell histiocytosis]].<ref name="Andrews">{{cite book |author=James, William D.; Berger, Timothy G.; et al. |title=Andrews' Diseases of the Skin: clinical Dermatology |publisher=Saunders Elsevier |location= |year=2006 |pages= |isbn=0-7216-2921-0 |oclc= |doi= |accessdate=}}</ref>{{rp|720}} | ||
==References== | ==References== | ||
{{ | {{Reflist|2}} | ||
[[Category:Disease]] | [[Category:Disease]] | ||
{{WH}} | {{WH}} | ||
{{WS}} | {{WS}} | ||
Latest revision as of 12:48, 17 October 2012
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Synonyms and keywords: Congenital self-healing reticulohistiocytosis; Hashimoto-Pritzker disease
Overview
Hashimoto–Pritzker syndrome is a condition that is a self-limited form of Langerhans cell histiocytosis.[1]:720
References
- ↑ James, William D.; Berger, Timothy G.; et al. (2006). Andrews' Diseases of the Skin: clinical Dermatology. Saunders Elsevier. ISBN 0-7216-2921-0.