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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...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Pediatr Gastroenterol Hepatol Nutr |
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| Κύριοι συγγραφείς: | , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition
2019
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| Θέματα: | |
| Διαθέσιμο Online: | 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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