Pancytopenia in a patient with cystinosis secondary to myelosuppression from cystine crystal deposition: a case report

INTRODUCTION: Cystinosis is a rare metabolic genetic disorder caused by a mutation in the cystinosin lysosomal cystine transporter gene. Clinically, it is characterized by systemic accumulation of cystine crystals in tissues causing end-organ dysfunction in the kidney, eyes, muscles, and other organ...

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Detalles Bibliográficos
Autores principales: Lyou, Yung, Zhao, Xiaohui, Nangia, Chaitali S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573917/
https://www.ncbi.nlm.nih.gov/pubmed/26377065
http://dx.doi.org/10.1186/s13256-015-0691-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573917/
https://www.ncbi.nlm.nih.gov/pubmed/26377065
http://dx.doi.org/10.1186/s13256-015-0691-8

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