Indication
Nephropathic cystinosis
Nephropathic cystinosis is a rare, severe autosomal recessive lysosomal storage disease caused by pathogenic variants in the *CTNS* gene, which impairs the carrier protein cystinosin and results in systemic accumulation of cystine crystals within cellular lysosomes. Read more about Nephropathic cystinosis
6 drugs 4 manufacturers
Drugs that treat it
Common Nephropathic cystinosis therapies.
PROCYSBI (cysteamine bitartrate)
PROCYSBI (cysteamine bitartrate)
PROCYSBI (cysteamine bitartrate)
PROCYSBI (cysteamine bitartrate)
PROCYSBI (cysteamine bitartrate)
News & literature
Coming soonRelated codes
Coming soonRelated conditions & guidelines
Coming soonNephropathic cystinosis is a rare, severe autosomal recessive lysosomal storage disease caused by pathogenic variants in the *CTNS* gene, which impairs the carrier protein cystinosin and results in systemic accumulation of cystine crystals within cellular lysosomes.
It predominantly manifests in infancy, presenting primarily with renal Fanconi syndrome—marked by proximal tubular dysfunction leading to severe urinary loss of fluids, electrolytes, and nutrients, alongside failure to thrive and hypophosphatemic rickets.
Without timely intervention, progressive renal parenchymal damage advances to end-stage kidney disease during childhood.
Over time, multiorgan accumulation of cystine leads to prominent extrarenal manifestations, including corneal crystal deposition with photophobia, hypothyroidism, neuromuscular dysfunction, and endocrine abnormalities.
- nih.gov
Nephropathic cystinosis is a rare, severe autosomal recessive lysosomal storage disease caused by pathogenic variants in the *CTNS* gene, which impairs the carrier protein cystinosin and results in systemic accumulation of cystine crystals within cellular lysosomes Without timely intervention, progressive renal parenchymal damage advances to end-stage kidney disease during childhood Over time, multiorgan accumulation of cystine leads to prominent extrarenal manifestations, including corneal crys...
- kidney.org
Nephropathic cystinosis is a rare, severe autosomal recessive lysosomal storage disease caused by pathogenic variants in the *CTNS* gene, which impairs the carrier protein cystinosin and results in systemic accumulation of cystine crystals within cellular lysosomes
- medlineplus.gov
It predominantly manifests in infancy, presenting primarily with renal Fanconi syndrome—marked by proximal tubular dysfunction leading to severe urinary loss of fluids, electrolytes, and nutrients, alongside failure to thrive and hypophosphatemic rickets
- understandingcystinosis.com
It predominantly manifests in infancy, presenting primarily with renal Fanconi syndrome—marked by proximal tubular dysfunction leading to severe urinary loss of fluids, electrolytes, and nutrients, alongside failure to thrive and hypophosphatemic rickets
- cystinosis.org
Without timely intervention, progressive renal parenchymal damage advances to end-stage kidney disease during childhood
- orpha.net
Over time, multiorgan accumulation of cystine leads to prominent extrarenal manifestations, including corneal crystal deposition with photophobia, hypothyroidism, neuromuscular dysfunction, and endocrine abnormalities
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