ArticleCase reports in pediatrics2015
Klippel-Trenaunay Syndrome with Extensive Lymphangiomas.
Article in Case reports in pediatrics, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
What it found
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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.
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.
Who cites it
9 citing papers in PubMed, 16 citations in OpenAlex.
- A phase 2 randomized, double-blind trial of ART-001, a selective PI3Kα inhibitor, for the treatment of slow-flow vascular malformations.Orphanet journal of rare diseases · 2025Trial
- Klippel-Trenaunay Syndrome in the Distal Part of the Unilateral Upper Limb and Venous Deficiency: A Case Report.JNMA; journal of the Nepal Medical Association · 2025Article
- A Case of Klippel-Trenaunay Syndrome With Gastrointestinal Hemorrhage and Splenomegaly.Cureus · 2024Article
- A Rare Case of Klippel Trenaunay Syndrome with Von Willebrand Factor Deficiency and Multiple Accessory Spleens: A Case Report and Brief Literature Review.Advanced biomedical research · 2024Article
- Klippel-Trenaunay Syndrome.Internal medicine (Tokyo, Japan) · 2023Article
- Abnormal uterine bleeding in a female with Klippel Trenaunay syndrome.Archive of clinical cases · 2022Article
- Radiological Aspect of Klippel-Trénaunay Syndrome: A Case Series With Review of Literature.Current medical science · 2018Article
- Lymphangiomatosis With Hemihypertrophy.Global pediatric health · 2016Article
- Klippel-Trenaunay and Parkes-Weber syndromes: two case reports.Jornal vascular brasileiroArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Klippel-Trenaunay syndrome (KTS) is a rare disorder characterized by the triad of vascular malformations, venous varicosities, and bone and soft-tissue hypertrophy. We present a case of Klippel-Trenaunay syndrome with limb hypertrophy, port-wine stains, lymphangiomas, and venous varicosities in the limbs.
Identifiers
What OpenQuestion holds
Registered trials
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.