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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...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Dove
2022
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| Materias: | |
| 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 |