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T. van Meurs, J. van Hagen, M. van de Scheur, H. Vermaat, M. Ruijs, H. van den Hoogenband, et al., “Classic Pseudoxanthoma Elasticum in a Patient with Sickle Cell Disease,” Journal of the American Academy of Dermatology, Vol. 56, No. 1, 2007, pp. 170-171. doi:10.1016/j.jaad.2006.10.023

has been cited by the following article:

• TITLE: Cutaneous Manifestations of Sickle Cell Disease

  AUTHORS: Heather Jones, Morey Blinder, Milan Anadkat

  KEYWORDS: Sickle Cell Disease; Leg Ulcers; Pseudoxanthoma Elasticum; Nitric Oxide Deficiency; Hydroxyurea

  JOURNAL NAME: Open Journal of Blood Diseases, Vol.3 No.3, September 16, 2013

  ABSTRACT: Sickle cell disease is an inherited erythrocyte disorder affecting multiple organ systems. As individuals are living well into middle age due to advances in diagnosis and treatment, further disease-related complications are being recognized. This article reviews the cutaneous manifestations of sickle cell disease including leg ulcers and acquired pseudoxanthoma elasticum.