ORPHA:228247
Acquired pseudoxanthoma elasticum
Also known as: Acquired Gronblad-Strandberg-Touraine syndrome · Acquired PXE
Query health: suspect — Only one of 2 strategies returned hits (phrase).
Publications
28
24.9th percentile
Trials
0
Interventional, condition-specific
Researchers
119
Distinct authors in sample
Gene link
—
Readiness
1/6
Stages with a signal
Clinical definition (Orphanet)
A rare acquired dermis elastic tissue disorder characterized by clinical and histopathologic evidence of pseudoxanthoma elasticum in the absence of a family history or specific mutation. Patients present with predominantly cutaneous manifestations consisting of yellowish papules which coalesce into large plaques and are most commonly localized on the neck, axillae, groin, and flexural surfaces. Skin biopsy shows accumulation of clumped, calcified elastic fibers in the mid-dermis. Reported underlying factors include previous liver transplantation, exposure to penicillamine, or concomitant beta-thalassemia.
How rare: <1 / 1 000 000 — fewer than one in a million. In a city the size of Kolkata, that might mean on the order of fifteen people.
Cross-references
Joined from Mondo / Orphanet. MeSH labels may enter searches; UMLS / OMIM / NCIT are stored for reference.
- MONDO:0016441
- UMLS:C1274759
Additional Mondo synonyms (6)
acquired Gronblad-Strandberg-Touraine syndrome · acquired PXE · acquired pseudoxanthoma elasticum · acquired pseudoxanthoma elasticum (inherited or acquired) · localised acquired cutaneous pseudoxanthoma elasticum · localized acquired cutaneous pseudoxanthoma elasticum
Research stages
Trial readiness signals
Where this condition sits on an open-data research pipeline — not how close a treatment is, and not medical advice. Empty stages often mean “not in these databases under this Mondo ID,” not “impossible.”
1/6 stages with a signal
Research-stage checklist from open sources (GenCC, literature, Monarch when enriched, ClinicalTrials.gov). Not a prognosis or care recommendation.
- Gene identifiedNot found
No GenCC disease–gene assertion in this build
- LiteraturePresent
28 matched papers (8 in last 10 years) Source
- Phenotype characterisedNot checked
Not yet enriched from Monarch / HPO
- Animal modelNot checked
Not yet enriched from Monarch / Alliance
- Orphan designationNot checked
FDA/EMA orphan-drug designation not enriched yet
- Interventional trialNot found
No matched interventional trial under our ClinicalTrials.gov rules
Biology
Genes and phenotypes
Gene–disease validity from GenCC, plus phenotypes and animal models joined from Monarch Initiative via Mondo ID — not a clinical diagnosis aid.
Do we know what causes it?
Not yet — the cause hasn't been pinned down in GenCC.
No strong gene–disease assertion joined for this Orphanet entity.
Phenotypes (Monarch / HPO)
Not enriched in this build — Monarch phenotype joins were not run for this record.
Animal models (Monarch / Alliance)
Not enriched in this build.
Literature
Is anyone studying this?
28
28 papers have ever been published on this condition (under this name). For scale, breast cancer has over 700,000. Median papers in the last 10 years for a rare disease in this dataset (publications denominator n=5449) is 41.
28 papers since the earliest indexed year in this search — median last-10-year count for a rare disease in this dataset is 41 (publications denominator n=5449).
8 in the last 10 years · high confidence · 24.9th percentile (publications denominator)
Phrase hits: 28 · MeSH hits: 0
Who's working on it?
119
Distinct author names in 28 sampled papers — named people below.
Who's working on it?
No interventional trial matched this name; these authors publish on it in the sampled literature — a practical starting point for contact.
- 01Martin L4 papers · 2025
MitoVasc Institute, UMR CNRS 6015/INSERM 1083, 49100, Angers, France.
Papers in Europe PMC - 02Bercovitch L3 papers · 2011
Department of Dermatology, Rhode Island Hospital and Warren Alpert Medical School of Brown University, Providence, Rhode Island 02903, USA. Lionel_Bercovitch@brown.edu
Papers in Europe PMC - 03Terry SF3 papers · 2011Papers in Europe PMC
- 04Bessis D2 papers · 2025
Department of Dermatology, Montpellier University Hospital, Montpellier, France.
Papers in Europe PMC - 05Chassaing N2 papers · 2011
Department of Medical Genetics, INSERM U563, Purpan Hospital, Toulouse, France.
Papers in Europe PMC - 06De Paepe A2 papers · 2012Papers in Europe PMC
- 07Hosen MJ2 papers · 2012
Center for Medical Genetics, Ghent University Hospital, De Pintelaan 185, 9000 Ghent, Belgium ; Department of Genetic Engineering and Biotechnology, Shahjalal University of Science and Technology, Sylhet 3114, Bangladesh.
Papers in Europe PMC - 08Le Saux O2 papers · 2025
Department of Cell and Molecular Biology, John A. Burns School of Medicine, University of Hawaii, Honolulu, HI, USA.
Papers in Europe PMC - 09Terry PF2 papers · 2011Papers in Europe PMC
- 10Uitto J2 papers · 2011
Department of Dermatology and Cutaneous Biology, Jefferson Medical College, Thomas Jefferson University, Philadelphia, Pennsylvania, USA. jouni.uitto@jefferson.edu
Papers in Europe PMC
Clinical research
Is a treatment being tested?
0
interventional trials for this specific condition
No interventional trial testing a treatment matched this specific condition name on ClinicalTrials.gov (observational studies and pan-disease registries are listed separately when present).
Data as of 27 July 2026
No matched interventional trials. This is true for 73% of diseases in the trials denominator (5114 of 7003). Here are the researchers publishing on it.
high confidence · 36.5th percentile (trials denominator)
Recruiting interventional trials
From the matched ClinicalTrials.gov set
No interventional trial testing a treatment was found for this specific condition name on ClinicalTrials.gov.
See who's working on it — people publishing on this disease are often the practical next contact when no trial is listed.
Where to find support
We do not yet link condition-specific patient organisations. These umbrella groups support undiagnosed and ultra-rare families:
India — NPRD
Last verified 2026-07-26This ORPHAcode is not on our curated NPRD list (direct or Mondo-parent match). That does not decide clinical eligibility; families in India should ask a notified Centre of Excellence about current coverage.
Hand-curated for this project. ORPHAcode mappings are best-effort and may be incomplete or imprecise for umbrella categories. Parent (Mondo) matches mean the policy lists a broader category — confirm eligibility with a Centre of Excellence. Financial entitlements summarised from public policy statements and may change. This is not official government guidance.
How we counted this
Europe PMC query (preferred label + any corrected label + Orphanet and Mondo exact synonyms, stoplisted; unioned with resolved MeSH labels when available). UMLS / OMIM / NCIT cross-references are stored on the overview but are not added to the query string.
"Acquired pseudoxanthoma elasticum" OR "Acquired Gronblad-Strandberg-Touraine syndrome" OR "Acquired PXE" OR "acquired pseudoxanthoma elasticum (inherited or acquired)" OR "localised acquired cutaneous pseudoxanthoma elasticum" OR "localized acquired cutaneous pseudoxanthoma elasticum"
ClinicalTrials.gov query (quoted phrases + MeSH via query.cond, plus recall-expansion terms when used):
"Acquired pseudoxanthoma elasticum" OR "Acquired Gronblad-Strandberg-Touraine syndrome" OR "Acquired PXE" OR "acquired pseudoxanthoma elasticum (inherited or acquired)" OR "localised acquired cutaneous pseudoxanthoma elasticum" OR "localized acquired cutaneous pseudoxanthoma elasticum" OR "pseudoxanthoma elasticum (inherited or acquired)"
Recall-expansion terms: pseudoxanthoma elasticum (inherited or acquired)
Study-type breakdown: 0 interventional · 0 observational · 0 expanded access. Only interventional studies enter the trial headline.
Query health: suspect — strategies attempted: phrase, recall-expansion; with hits: phrase
Run this search on ClinicalTrials.gov
Confidence reasoning
- Preferred label is multi-word and distinctive
- No synonyms dropped by stoplist
- No label/synonym collisions with other diseases in this corpus
Ingested 2026-07-27T10:05:07.819Z