Prolidase deficiency associated with systemic lupus erythematosus (SLE): single site experience and literature review

INTRODUCTION: Prolidase deficiency (PD) is a rare autosomal recessive disorder which may have a wide spectrum of clinical features. These features include a characteristic facies, cognitive impairment, rashes or skin ulceration, splenomegaly, recurrent infections involving mainly the respiratory sys...

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Detalles Bibliográficos
Autores principales: Butbul Aviel, Yonatan, Mandel, Hana, Avitan Hersh, Emily, Bergman, Reuven, Adiv, Orly Eshach, Luder, Anthony, Brik, Riva
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623899/
https://www.ncbi.nlm.nih.gov/pubmed/22726576
http://dx.doi.org/10.1186/1546-0096-10-18

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3623899/
https://www.ncbi.nlm.nih.gov/pubmed/22726576
http://dx.doi.org/10.1186/1546-0096-10-18

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