Xanthoma Disseminatum In a Pair of Blind, Deaf Male Twins
Author(s) -
Naveed Natanzi,
David H. Peng,
Eli Ahdoot,
Sandra Ghatan,
Amy Reinstandler,
Ramin Ram
Publication year - 2011
Publication title -
isrn dermatology
Language(s) - English
Resource type - Journals
eISSN - 2090-4606
pISSN - 2090-4592
DOI - 10.5402/2011/342909
Subject(s) - histiocyte , etiology , xanthoma , dermatology , medicine , pathology , inheritance (genetic algorithm) , biology , genetics , gene
Xanthoma disseminatum (XD) is a rare normolipemic histiocytic disorder of non-Langerhans cell origin characterized by erythematous to tan/brown papules in flexor surfaces. Considered a generally benign, chronic disease of unknown etiology, XD typically affects the skin, mucous membranes, and less commonly, other organs. To date, there has been no typical or consistent inheritance pattern described, nor has it ever been considered as a component of any known syndrome. We describe, for the first time, two cases of XD in a pair of blind and deaf twin brothers.
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