Hashimoto-Pritzker syndrome: Difference between revisions
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{{SK}} Congenital self-healing reticulohistiocytosis; Hashimoto-Pritzker disease | |||
==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== | |||
{{Reflist|2}} | |||
[[Category:Disease]] | |||
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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.