Wilson Disease Comorbid with Hereditary Sensory Autonomic Neuropathy Type IV and Gitelman Syndrome

Wilson disease a rare autosomal recessive inherited disorder of copper metabolism, is characterized by excessive deposition of copper in the liver, brain, and other tissues. Wilson disease is often fatal if it is not recognized early and treated when it is symptomatic. Gitelman syndrome is also an a...

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Detalles Bibliográficos
Autores principales: Kim, Ju Young, Park, Sung Sup, Yang, Hye Ran
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629596/
https://www.ncbi.nlm.nih.gov/pubmed/31338315
http://dx.doi.org/10.5223/pghn.2019.22.4.392

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6629596/
https://www.ncbi.nlm.nih.gov/pubmed/31338315
http://dx.doi.org/10.5223/pghn.2019.22.4.392

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