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Familial homozygous hypercholesterolemia with arcus cornea and xanthomas: A rare but serious entity

Familial homozygous hypercholesterolemia with arcus cornea and xanthomas: A rare but serious entity

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_81354690dec84609a5545df232def7f5

Familial homozygous hypercholesterolemia with arcus cornea and xanthomas: A rare but serious entity

About this item

Full title

Familial homozygous hypercholesterolemia with arcus cornea and xanthomas: A rare but serious entity

Publisher

England: John Wiley & Sons, Inc

Journal title

Clinical case reports, 2023-03, Vol.11 (3), p.e7024-n/a

Language

English

Formats

Publication information

Publisher

England: John Wiley & Sons, Inc

More information

Scope and Contents

Contents

Familial hypercholesterolemia (FH) is a rare but life‐threatening disorder. Skin manifestations can be its only manifestation. We present a case of a fifteen‐year‐old female child, with multiple eruptive xanthomas, xanthomas anarcus, and a deranged lipid profile consistent with FH. The presence of this manifestation especially in the younger age gr...

Alternative Titles

Full title

Familial homozygous hypercholesterolemia with arcus cornea and xanthomas: A rare but serious entity

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_doaj_primary_oai_doaj_org_article_81354690dec84609a5545df232def7f5

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_doaj_primary_oai_doaj_org_article_81354690dec84609a5545df232def7f5

Other Identifiers

ISSN

2050-0904

E-ISSN

2050-0904

DOI

10.1002/ccr3.7024

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