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Newborn New York NY

Receiving the news that your baby has been diagnosed with a rare congenital disorder can be alarming. Suddenly, the future looks daunting and filled with uncertainty. While Klippel–Trenaunay Syndrome (KTS) is rare, it can be managed, and your healthcare team will do everything possible to help prevent complications.

KTS involves irregular development of the blood vessel, skin, muscles, bones and lymphatic system. A red birthmark, generally called a port-wine stain, along with overgrowth of tissues, vein malformations and bone overgrowth are signs. There may or may not be lymphatic abnormalities as well.

Be Aware of Complications

Babies who are born with KTS are usually diagnosed at birth. Accurate diagnosis is important. When KTS has been confirmed, it is important to get the necessary care to address any symptoms and prevent complications.

Problems can develop due to the abnormal development of the blood vessels, bones, soft tissues and lymphatic system. Bleeding from thickened port-wine stain areas is possible. Vein malformations can cause various problems, some of which may be painful. Bone overgrowth can also lead to complications in some instances. Lymphedema, a buildup of fluid, can cause swelling in the arms or legs. Your doctor will advise you of which symptoms to be aware.

Working with Your Child’s Healthcare Team

Because KTS can involve more than one system in the body, the health care team will most likely include specialists from various fields of medicine. Together, you and the team will develop the best treatment plan for your child.

A partial list of treatments includes physical therapy, compression therapy, orthopedic devices, laser ablation of veins, surgery and medication. Your child may require one of these or some other type of care. Treatment modalities will depend on the type of complication needing to be addressed. It is crucial for you to keep appointments and follow the doctor’s recommendations. If you notice any changes, you should notify your doctor.

Getting Support

KTS can be a challenging condition; however, you have the support of your health care team, and there are advocacy and support groups to provide additional encouragement, resources and information. Remember, you do not have to embark on this journey alone.

The Vascular Birthmark Center has expertise and experience working with KTS patients. Contact us for a consultation appointment for more information about this rare condition.

Posted on behalf of The Vascular Birthmark Center

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Our Patient Reviews
The Vascular Birthmark Center: Gregory M. Levitin, MD

4.8 / 5.0

Based on 27 reviews

Abril M.

Dr. Levitin is very knowledgeable, compassionate and professional. Five years ago, I needed to find information about a birth mark that my newborn daughter started to grow a couple days after birth. I was afraid, I did not feel like I got any clear information about it through my insurance; also, they did not offer any course of treatment for it. I started to look for information, the birthmark was growing each day, information was scarce and I just got more scared. Finally, I found a video in Youtube from a grandmother who was very grateful after finding treatment for her grand daughter through The Birthmark Foundation. It was a huge blessing to me and my family. I found Dr. Levitin, I contacted him thinking he probably would not even answer. I was wrong, he kindly answered promptly, got in touch with me and soon he had a plan : ) I went to see him at the Birthmark Center in Los Angeles. He explained everything in a way that it was so clear to understand, no question I made was insignificant and his answers were each very informative. I really never have had an experience with a doctor who explains and speaks in such a way. I left his office knowing that my daughter was in the best hands and the best care. I first thank God for the Birthmark Foundation, a great organization with the highest quality of doctors. Also, a very special thanks to Dr. Levitin for all his help and kindness, for listening to my concerns and answering each and every question. And last, but no least, to the Birthmark Foundation Center in Los Angeles : ) I hope many children can find help/care in this place as I found it for my daughter. Thank you forever.

Ryan E.

I will be telling tales of the good doctors compassion till time comes to an end. Because of Dr Levitin, I have more confidence in my every day life. He was fast, knowledgeable, precise and all with a disarming sense of humor. Two thumbs up!

Carla M.

I wanted to show you how much better Hailey's tongue looks and let you know her speech has already improved so much!!! Her speech teacher is thrilled!!!! Thank you so much for everything you did for her. You are an excellent surgeon with a great bedside manner- we are forever grateful to you!!! We are so appreciative!

Danielle L.

we are forever grateful for Dr. Levitin. My daughter Lena had surgery to remove her hemangioma that was located on her forehead at just 6 month old. she healed beautifully and we couldn't be happier with how minimal her scar is, even almost 4.5 years later. Dr. Levitin is caring, compassionate, and such a great doctor/surgeon overall. He had our daughter's best interest and I knew she was in good hands. I highly recommend him any chance I get!

Chris

My name is Chris and I was recently treated for an AVM on my forehead by Dr. Gregory Levitin of New York (New York Eye and Ear Infirmary). Thankfully, I live within a few hours of NYC. In brief, I would like to say that Dr. Levitin is very capable doctor with a lot of experience with AVMs. He responds quickly to e-mail, texts, and phone calls. He accepts insurance. He takes a "team approach" and will be your "QB" and involve other specialists as necessary. In my particular case they were Dr. Raj Shrivastava (Mt Sinai) and Dr. Raphael A. Ortiz (Lenox Hill) in NY. I recommend contacting Dr Levitin for a consultation if you suspect you have an AVM. All 3 Drs are just good people. When I spoke to them, they treated me like like an equal. I felt like they were advising me as a close friend or family member. Like many that suffer with AVMs I was at first mis-diagnosed. What was thought to be a just a simple cyst turned out to be an AVM. Surgery to remove the cyst made the AVM about 5x bigger. My treatment entailed a few MRIs and CAT scans to determine what was going on and the treatment plan. This was followed by consultation with the 3 Drs mentioned above and finally a 2-day procedure. On day 1 Dr Ortiz embolized the AVM. On day 2 Dr Levitin and Dr Shrivastava removed the AVM from my skull and put some metal mesh there to fill the "hole". It has been 6-months since the surgery and so far I have not had any recurrence. In honor of Vascular Birthmark Awareness Day and to thank these Drs for all they have done for me, I just want to give everyone a solid reference. Finding the right doctor for this type of stuff makes all the difference.

Valle S.

I just discovered this page i have also a birthmark I always experiences bully because of this. I don't know what kind of birthmark is this if it is harmful ? I hope Dr. Levitin notice this message in this way I think he can help me :) :) #DrLevitin

Alicia M.

This year marks the 10th that I contacted VBF for help. Since then I have been under the care of Dr. G Levitin and Dr. R. Ortiz, they are my guardian healing angels! Thanks VBF for not only helping me but also for letting me be a volunteer in the foundation whenever I am needed. A Big Hug to all from MIAMI... Alicia

Alexander G.

Totally positive experience. Dr. Levitin is a great professional. He has diagnosed and treated my nose breathing problem, significantly improving my quality of life. Office staff is very professional. Appointments always kept on time. Strongly recommend.