Answers are grounded in this paper and cite their sources.
Klippel-Trenaunay syndrome (KTS) is a rare congenital disorder characterized by a port-wine stain birthmark, venous anomalies, and soft-tissue hypertrophy. Diagnosis of KTS is made based on two of the three characteristic diagnostic features. Klippel-Trenaunay syndrome is unilateral and more commonly affects the lower extremities. This case report describes a unique patient who lacked a patent deep system in the affected limb, making the traditional treatment of varicosities a dangerous outcome for this patient.
No takes yet. Share an insight, caveat, or question.
Paris et al. (2024) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: