| Literature DB >> 18489053 |
Ammar M Ahmed1, Nazila Barahmani, Madeleine Duvic.
Abstract
Alopecia areata (AA) has a strong hereditary component and is associated with a number of other autoimmune diseases. There is no established relationship between AA and any of the congenital thrombocytopenias. 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.Entities:
Mesh:
Year: 2008 PMID: 18489053 DOI: 10.1016/j.jaad.2007.05.017
Source DB: PubMed Journal: J Am Acad Dermatol ISSN: 0190-9622 Impact factor: 11.527