Difficult Journey to Find the Best Treatment for Homozygous Familial Hypercholesterolemia: Case Report

Homozygous familial hypercholesterolemia (HoFH) is a rare autosomal recessive genetic disorder. It is difficult to diagnose and treat it at early stage. We present a nine-year-old boy with HoFH from China. At the beginning, he was misdiagnosed as xanthomatosis in the dermatology department of the lo...

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Detalles Bibliográficos
Autores principales: Xu, Ming-Jun, Chu, Jian-Ping, Fei, Wen-Ling, Wang, Juan, Zhang, Yan-Min, Wang, Yi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956246/
https://www.ncbi.nlm.nih.gov/pubmed/35340792
http://dx.doi.org/10.2147/IMCRJ.S345320

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8956246/
https://www.ncbi.nlm.nih.gov/pubmed/35340792
http://dx.doi.org/10.2147/IMCRJ.S345320

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