Phenotypic Spectrum and Diagnostic Challenges in Klippel‐Trenaunay Syndrome: A Case Series
Klippel-Trénaunay syndrome (KTS) is a rare congenital disorder characterized by the triad of capillary malformations, venous varicosities, and soft tissue or bony hypertrophy. This case series highlights rare and atypical presentations of KTS, emphasizing the importance of a multidisciplinary diagnostic approach.
Authors
- Md Ariful Haque (ORCID: https://orcid.org/0000-0003-4632-5153)
- Tooba Ali (ORCID: https://orcid.org/0000-0003-1867-943X)
- Marya Hameed (ORCID: https://orcid.org/0000-0002-1867-8755)
Institutions
- Jinnah Sindh Medical University (PK)
- Atish Dipankar University of Science and Technology (BD)
- Dow University of Health Sciences (PK)
- National Institute of Child Health (PK)
Publication Details
- Journal
- Clinical Case Reports
- Published
- 2025-11-01
- DOI
- https://doi.org/10.1002/ccr3.71482
- Primary Topic
- Vascular Malformations and Hemangiomas
- Type
- article
- Field-Weighted Citation Impact
- 0.00