Evidence map›Paper›PMID 36879675›Full record

ArticleClinical case reports2023

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

Amal Chamli, Anissa Zaouak, Refka Frioui, Samy Fenniche, Houda Hammami

Open access · goldAbstract readCase Reports
In one paragraph

Article in Clinical case reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 33% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Amal ChamliDermatology Department Habib Thameur Hospital Tunis Tunisia.ORCID https://orcid.org/0000-0002-7927-9088
Anissa ZaouakDermatology Department Habib Thameur Hospital Tunis Tunisia.ORCID https://orcid.org/0000-0003-2062-2256
Refka FriouiDermatology Department Habib Thameur Hospital Tunis Tunisia.ORCID https://orcid.org/0000-0001-9441-2070
Samy FennicheDermatology Department Habib Thameur Hospital Tunis Tunisia.
Houda HammamiDermatology Department Habib Thameur Hospital Tunis Tunisia.
Tunis University · TN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 group should draw attention to hypercholesterolemia. A timely diagnosis is fundamental to prevent serious complications and for early treatment.

Indexed as

corneafamilial hypercholesterolemiahomozygoushypercholesterolemiaxanthomatosis

Identifiers

PMID36879675
PMCPMC9984865
OpenAlexW4323050048

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.