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Klippel Trenaunay syndrome.

Nadeem Alam Zubairi1, Arfan ul Bari, Tariq Mahmood

  • 1Department of Paediatrics, PAF Hospital, Sargodha, Pakistan. nadeem_alam61@hotmail.com

Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
|July 29, 2004
PubMed
Summary

Klippel-Trenaunay syndrome (KTS) is a rare congenital vascular disorder. This case study details a young girl diagnosed with KTS, highlighting its key characteristics.

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Area of Science:

  • Vascular Medicine
  • Pediatric Genetics
  • Congenital Disorders

Background:

  • Klippel-Trenaunay syndrome (KTS) is a rare congenital vascular malformation disorder.
  • Etiology remains largely unknown, presenting diagnostic challenges.
  • Characterized by a triad of capillary malformations (port-wine stains), venous malformations, and hypertrophy of affected limbs.

Observation:

  • A case presentation of KTS in a young female patient is described.
  • The patient exhibited typical clinical manifestations of the syndrome.
  • Detailed clinical observations and diagnostic findings are noted.

Findings:

  • The diagnosis of Klippel-Trenaunay syndrome was confirmed in the pediatric patient.
  • The case illustrates the complex presentation of vascular anomalies and limb overgrowth.
  • Clinical findings align with established diagnostic criteria for KTS.

Implications:

  • This case contributes to the understanding of KTS in pediatric populations.
  • Highlights the importance of early diagnosis and multidisciplinary management for KTS.
  • Underscores the need for further research into the genetic and molecular basis of KTS.

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