Xanthomas Can Be Misdiagnosed and Mistreated in Homozygous Familial Hypercholesterolemia Patients: A Call for Increased Awareness Among Dermatologists and Health Care Practitioners

• প্রধান লেখক: Fahad Alnouri (লেখক), Faisal A. Al-Allaf (লেখক), Mohammad Athar (লেখক), Zainularifeen Abduljaleel (লেখক), Moheeb Alabdullah (লেখক), Dalal Alammari (লেখক), Menwar Alanazi (লেখক), Fahmi Alkaf (লেখক), Abeer Allehyani (লেখক), Mohammad A. Alotaiby (লেখক), Abdullah Alshehri (লেখক), Abdellatif Bouazzaoui (লেখক), Hussam Karrar (লেখক), Mohiuddin M. Taher (লেখক)
• বিন্যাস: গ্রন্থ
• প্রকাশিত: Ubiquity Press, 2020-02-01T00:00:00Z.
• বিষয়গুলি: article
• অনলাইন ব্যবহার করুন: Connect to this object online.

Background: Familial hypercholesterolemia (FH) is an autosomal dominant inherited genetic disorder and results in the development of coronary artery disease (CAD). Clinical diagnosis of homozygous HH patients is usually straightforward because persistent hypercholesterolemia can produce xanthoma and...