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OrphanAnesthesia
S.E. George

Klippel-Trénaunay syndrome

Klippel-Trénaunay syndrome

Schlüsselwörter Klippel-Trénaunay syndrome; ICD 10: Q87.2; Angio osteohypertrophy, naevus vasculosus osteohypertrophicus, capillary lymphatic venous malformation (CLVM)
Keywords Klippel-Trénaunay syndrome; ICD 10: Q87.2; Angio osteohypertrophy, naevus vasculosus osteohypertrophicus, capillary lymphatic venous malformation (CLVM)
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Summary

Klippel-Trénaunay syndrome is a rare congenital malformation with an incidence of 1 out of 27,500 live births, characterised by a triad of venous malformations or varicose veins, cutaneous capillary malformations and bony or soft-tissue hypertrophy in affected limbs. The lung, trunk, gastrointestinal tract, neurovascular structures and the bladder may be involved with the presence of vascular malformations. 

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