Evidence map›Paper›PMID 40455211›Full record

ReviewDie Ophthalmologie2025

[Ocular alterations in pseudoxanthoma elasticum : The eye as a window to diagnosing a systemic disease].

Kristin Raming, Jonathan Meinke, Georg Ansari, Giuseppe Cancian, Katja Stürzebecher, Daniel Staub, Nicolas Feltgen, Frank G Holz, Maximilian Pfau, Kristina Pfau

Abstract readEnglish AbstractReview
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In one paragraph

Review in Die Ophthalmologie, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

10 authors.

Kristin RamingUniversitäts-Augenklinik Bonn, Universität Bonn, Venusberg-Campus-1, 53127, Bonn, Deutschland. Kristin.Raming@ukbonn.de.ORCID http://orcid.org/0000-0003-1133-8675
Jonathan MeinkeUniversitäts-Augenklinik Bonn, Universität Bonn, Venusberg-Campus-1, 53127, Bonn, Deutschland.
Georg AnsariAugenklinik, Universitätsspital Basel, Universität Basel, Basel, Schweiz.
Giuseppe CancianAugenklinik, Universitätsspital Basel, Universität Basel, Basel, Schweiz.
Katja StürzebecherAngiologie, Universitätsspital Basel, Universität Basel, Basel, Schweiz.
Daniel StaubAngiologie, Universitätsspital Basel, Universität Basel, Basel, Schweiz.
Nicolas FeltgenAugenklinik, Universitätsspital Basel, Universität Basel, Basel, Schweiz.
Frank G HolzUniversitäts-Augenklinik Bonn, Universität Bonn, Venusberg-Campus-1, 53127, Bonn, Deutschland.
Maximilian PfauUniversitäts-Augenklinik Bonn, Universität Bonn, Venusberg-Campus-1, 53127, Bonn, Deutschland.
Kristina PfauUniversitäts-Augenklinik Bonn, Universität Bonn, Venusberg-Campus-1, 53127, Bonn, Deutschland. Kristina.Pfau@ukbonn.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pseudoxanthoma elasticum (PXE) is an autosomal-recessive multisystem disease characterized by elastic fiber calcification in the skin, the cardiovascular system, and eyes. PXE is caused by biallelic mutations in the ABCC6 gene on chromosome 16, resulting in low inorganic pyrophosphate plasma levels. Typical ocular manifestations result from calcification of Bruch's membrane and include peau d'orange, angioid streaks, and comet-tail lesions. Advances in multimodal imaging have significantly improved the detection of these features. Ocular complications in PXE include the development of secondary neovascularization, which can be treated with anti-vascular endothelial growth factor (VEGF) injections. In cases of suspected PXE, genetic testing and genetic counseling should be performed for diagnostic confirmation. Early referral to a specialized center is essential. Interdisciplinary care and management of complications, particularly in collaboration with angiologists, are crucial for treating this multisystem disorder. Although no approved causal therapy for PXE currently exists to date, accurate and early diagnosis using phenotypic characteristics is critical. Early identification of other affected family members and timely treatment of secondary complications allow for better disease management and offer patients the opportunity to participate in ongoing clinical trials. Promising therapeutic options are currently emerging and may significantly improve management and prognosis in the future.

Indexed as

Pseudoxanthoma ElasticumAngioid StreaksATP-Binding Cassette, Sub-Family C ProteinsDiagnosis, DifferentialEarly DiagnosisGenetic TestingHumansABCC6 protein, humanATP-Binding Cassette, Sub-Family C ProteinsAngioid streaksBruch-membraneCalcificationDark adaptationMineralizationPeau d’orange

Identifiers

What OpenQuestion holds

Textmetadata
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.