ArticleUltrasound (Leeds, England)2020
Prenatal diagnosis of Klippel-Trenaunay syndrome: Series of four cases and review of the literature.
Article in Ultrasound (Leeds, England), 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 14 citations in OpenAlex.
- Article
- 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
- Prenatal Ultrasound Diagnosis of Klippel-Trenaunay Syndrome.Diagnostics (Basel, Switzerland) · 2023Article
- Update on Color Flow Imaging in Obstetrics.Life (Basel, Switzerland) · 2022Review
- Prenatal ultrasonographic findings in Klippel-Trenaunay syndrome: A case report.World journal of clinical cases · 2021Article
- A neonate with Klippel-Trénaunay syndrome: a case report.Journal of medical case reports · 2021Article
- Klippel-Trénaunay-Weber Syndrome: Prenatal Diagnosis and Review of the Literature.Journal of clinical ultrasound : JCUReview
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Authors and funding
3 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Klippel-Trenaunay syndrome is a rare disease with a classic triad of port wine stains, varicose veins, and bony and soft tissue hypertrophy of an extremity. The quality of life in these patients is significantly affected, making the prenatal diagnosis of Klippel-Trenaunay syndrome important. We present four prenatally diagnosed cases of this anomaly with a unique case of ectrodactyly of the hand in foetus with Klippel-Trenaunay syndrome. Such a combination has not been previously reported prenatally. A review of the literature for similar cases is also presented.
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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.