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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...

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Pubblicato in:J Med Case Rep
Autori principali: Lyou, Yung, Zhao, Xiaohui, Nangia, Chaitali S.
Natura: Artigo
Lingua:Inglês
Pubblicazione: BioMed Central 2015
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Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC4573917/
https://ncbi.nlm.nih.gov/pubmed/26377065
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13256-015-0691-8
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