TY  - CHAP
M1  - Book, Section
TI  - Klippel-Trénaunay Syndrome
A1  - Bissonnette, Bruno
A1  - Luginbuehl, Igor
A1  - Engelhardt, Thomas
PY  - 2019
T2  - Syndromes: Rapid Recognition and Perioperative Implications, 2e
AB  - It  is  a  rare  congenital  medical  condition  characterized  by  the  association  of  soft  tissue  and  bony  hypertrophy,  venous  malformations,  lymphatic  abnormalities,  and  cutaneous  capillary  malformations.  The  main  characteristics  that  confirm  the  diagnosis  are  port-wine  stains  (pathognomonic),  venous  and  lymphatic  malformations,  and  soft-tissue  hypertrophy  of  the  affected  limb.  Patients  affected  with  large  arteriovenous  malformations  may  be  at  risk  of  peripheral  thrombosis  causing  potentially  a  pulmonary  embolism.  
SN  - 
PB  - McGraw-Hill Education
CY  - New York, NY
Y2  - 2024/04/16
UR  - accesspediatrics.mhmedical.com/content.aspx?aid=1164075502
ER  -