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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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| Publicado en: | Pediatr Gastroenterol Hepatol Nutr |
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| Main Authors: | , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2019
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6629596/ https://ncbi.nlm.nih.gov/pubmed/31338315 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5223/pghn.2019.22.4.392 |
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