Cargando…
Posterior segment optical coherence tomography findings in a case of nephropathic cystinosis
Cystinosis is a rare autosomal recessive lysosomal storage disorder characterized by abnormal accumulation of intracellular cystine in various tissues including the brain, kidneys, bones, and eyes. Infantile nephropathic cystinosis is the most severe phenotype of cystinosis that has been associated...
Autor principal: | Al Abdulsalam, Omar |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7866722/ https://www.ncbi.nlm.nih.gov/pubmed/33575541 http://dx.doi.org/10.4103/1319-4534.305049 |
Ejemplares similares
-
Hirschsprung's disease with infantile nephropathic cystinosis
por: Mittal, Deepak, et al.
Publicado: (2015) -
Improving the prognosis of nephropathic cystinosis
por: Besouw, Martine TP, et al.
Publicado: (2014) -
Spectral domain optical coherence tomography-based retinochoroidal cystine crystal score: a window into infantile nephropathic cystinosis
por: Keidel, Leonie, et al.
Publicado: (2023) -
Ventricular noncompaction in a female patient with nephropathic cystinosis: a case report
por: Ahmed, Ibrar, et al.
Publicado: (2009) -
Diagnostic challenge in a patient with nephropathic juvenile cystinosis: a case report
por: Higashi, Satomi, et al.
Publicado: (2017)