ArticleJournal of medical case reports2021
A neonate with Klippel-Trénaunay syndrome: a case report.
Article in Journal of medical case reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 7 citations in OpenAlex.
- Klippel-Trenaunay syndrome presenting with bilateral chronic central serous chorioretinopathy: a case report.Journal of medical case reports · 2026Article
- Capillary malformations in unusual territory: Klippel-Trénaunay syndrome with penoscrotal involvement.Skin health and disease · 2026Article
- Extensive venolymphatic involvement in infantile Klippel-Trenaunay syndrome: A rare case from Ethiopia.Radiology case reports · 2025Article
- A rare case of a 5-year-old girl with Klippel-Trénaunay syndrome and a bleeding focal vulvar hemangioma in Uganda.Clinical case reports · 2024Article
- Large birth mark and unilateral swelling of the lower extremity in a young teenager.BMJ case reports · 2024Article
- Klippel-Trénaunay syndrome with profound abdominal lymphatic-venous malformation in a three-day-old newborn: a case report and literature review.Frontiers in pediatrics · 2024Article
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundKlippel-Trénaunay syndrome is a rare congenital capillary-lymphatic-venous condition characterized by the clinical triad of capillary malformations (port wine stains), varicose veins with or without venous malformations, and bony and/or soft-tissue hypertrophy. It has a very low incidence of about 1:100,000. CASE PRESENTATION: We report the case of 21-day-old neonate Black African female (born in Uganda) with Klippel-Trénaunay syndrome who presented with macrodactyly and ectrodactyly on the left foot, as well as numerous port wine stains on the left thoracoabdominal region and anteroposterior left lower limb. Color Doppler ultrasound examination of the left lower limb and abdomen revealed varicose veins without signs of arteriovenous fistula.
conclusionThe report presents the case of a neonate with a rare congenital vascular disorder type Klippel-Trénaunay syndrome.
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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.