Gaois

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  1. SOCIAL QUESTIONS|health|illness · SOCIAL QUESTIONS|health|medical science

    #634561

    IATE #1685972
    histicíotóis chealla Langerhans Reference Faomhadh an téarma seo mar chuid de Thionscadal Lex
    ga
    Histiozytose X | Langerhans-Zell-Histiozytose | Langerhans-Zell-Granulomatose
    de
    histiocytosis X | Langerhans cell histiocytosis | LCH | Langerhans' cell granulomatosis | histiocytosis X syndrome
    en
    Definition systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues Reference "Orphanet > Langerhans cell histiocytosis, http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=3768&Disease_Disease_Search_diseaseGroup=histiocytosis-X&Disease_Disease_Search_diseaseType=Pat&Disease(s)%20concerned=Langerhans-cell-histiocytosis--Histiocytosis-X-&title=Langerhans-cell-histiocytosis--Histiocytosis-X-&search=Disease_Search_Simple (7.7.2009)"
    Comment "A review of the older terminology used can be found at: Schajowicz F., Slullitel J. Eosinophilic granuloma of bone and its relationship to Hand-Schüller-Christian and Letterer-Siwe syndromes > Journal of Bone and Joint Surgery - British Volume, Vol 55-B, Issue 3, 545-565 > Archive > 1973 > August > Eosinophilic granuloma of bone, http://www.jbjs.org.uk/cgi/reprint/55-B/3/545 [29.1.2008]The newer classifications (WHO, ICD10, MeSH) can be found at: Wikipedia http://en.wikipedia.org/w/index.php?title=Histiocytosis (see under Classification) [29.1.2008]"
    histiocytose X | histiocytose à cellules de Langerhans
    fr