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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...
Autores principales: | Lyou, Yung, Zhao, Xiaohui, Nangia, Chaitali S. |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
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 |
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