Langerhans cell histiocytosis
Other Names for this Disease
- Eosinophilic granuloma (formerly)
- Hand-Schüller-Christian syndrome (formerly)
- Histiocytosis X
- Letterer-Siwe disease (formerly)
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Although Langerhans cell histiocytosis is generally considered a sporadic, non-hereditary condition, it has reportedly affected more than one individual in a family in a very limited number of cases (particularly identical twins).
Last updated: 12/2/2013
- Langerhans Cell Histiocytosis. Online Mendelian Inheritance in Man (OMIM). 2009; http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=604856. Accessed 2/18/2010.
- Arico M, Nichols K, Whitlock JA, Arceci R, Haupt R, Mittler U, Kuhne T, Lombardi A, Ishii E, Egeler RM, Danesino C. Br J Haematol. 1999; http://www.ncbi.nlm.nih.gov/pubmed/10606898?dopt=Abstract. Accessed 2/18/2010.