....We report a family in which multiple members are affected with AA and with a hereditary thrombocytopenia, most consistent with pseudo–von Willebrand disease. This raises the possibility of a genetic association between AA and one or more of the inherited thrombocytopenias, possibly both related to mutations in genes on chromosome 17.
Journal of the American Academy of Dermatology
National Alopecia Areata RegistryAmmar M. Ahmed, BA, Nazila Barahmani, MD, Madeleine Duvic, MD![]()
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