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Up to: Inborn disorder of amino acid transport · Nephropathic cystinosis
Juvenile nephropathic cystinosis
Nephropathic juvenile cystinosis is the intermediate form, in regards to severity and age of onset, of cystinosis, a metabolic disease characterized by an accumulation of cystine inside the lysosomes that causes damage in different organs and tissues, particularly in the kidneys and eyes.
This condition has no sub-types.