A Case of Megaspleen With Micrographism

Wilson disease is an inherited disorder of copper metabolism with an autosomal recessive inheritance pattern (hepatolenticular degeneration). In this case, a 13-year-old child was seen with overall exhaustion, sporadic abdominal discomfort, and shrinking handwriting during the previous 12 months. On...

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Detalles Bibliográficos
Autores principales: VR, Subrahmanyan, Joy, Deepu V, Sahu, Sweta, SK, Anagha, LNU, Abhishek, Roopeessh, Vempati, Chandra, Prerna, Venugopal, Vishal, Bansal, Sourav, Tandi, Rishman
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Internal Medicine
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576253/
https://www.ncbi.nlm.nih.gov/pubmed/36277582
http://dx.doi.org/10.7759/cureus.29270

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9576253/
https://www.ncbi.nlm.nih.gov/pubmed/36277582
http://dx.doi.org/10.7759/cureus.29270

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