Klippel-Trenaunay syndrome is a rare birth defect that affects the blood and lymph vessels. Common symptoms of the disorder include cysts and swelling of the skin, dilated veins, abnormally fast growth of an extremity and flattened, colored marks that cover a large area on the affected extremity.
These are known as capillary malformations and they do not go away. As the child grows, so will the marks. The affected extremity will generally be painful and have a heavy sensation. Because the affected extremity will grow at an increased rate, problems may arise due to the difference in size. Blood clots and skin infections are common and can present complications.
Prenatal ultrasound can reveal the syndrome due to an enlarged limb. If the diagnosis is not made prenatally, it will be easily seen after the child is delivered.
There is no cure for Klippel-Trenaunay syndrome, but there are a variety of treatment options available. Surgery can performed to correct the excessive growth of the extremity and in severe cases, amputation may be required. Affected veins can be shrunk or removed and compression garments can be worn to decrease the amount of pain and swelling that the child may experience.
Comments: Klippel-Trenaunay-Syndrome
Comments 1 to 5 of about 5.
stcatherineofsiena -
515 days ago.
My daughter does't have this syndrome, we just found out!! It was worth the trouble of an MRI.
stcatherineofsiena -
733 days ago.
My daughter was born with a large port wine stain on her thigh and buttock. She is 10 months old now & her specialist realised her leg with the stain was larger than her other leg. I never noticed?? She will be having an MRI in July to look under her port wine stain. She possible has Klippel-Trenanay syndrome. We will have to wait & see!
ktbbaby -
797 days ago.
my sister has this! i am so surprised to find it here as it is pretty rare.
(and she is in her 30s and fine!)
she tried laser surgery and it did not fade the marks.
this has rarely impacted her.
clairebear87 -
832 days ago.
my son also has had this since birth although we only received the diagnosis today (he turned 1 last week), it is nice to find someone who is not in pain with it and doing well as i am beside myself with worry, even the doctor who diagnosed it didnt seem to know much about it, i have so many questions and dont know where to turn. My son is walking fine and doesnt seem to have any pain, his leg actually has faded alot since birth , it is a little bit wider than the other but not any longer,
Mommy-Nguyen -
1055 days ago.
My oldest son is almost 7 yrs old. He has this syndrome. He does not have any hypertrophy (where one limb is larger than the other) he does have a port wine Stain (red birth mark) that covers his entire left arm and part of his chest and back. It is from tangeled blood vessels. He has had no problems with this arm at all and laser surgery is not guaranteed to work, so why put him through the pain? He is doing wonderful, I see nothing different with him...
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