Top News

Symptoms of Cloves Syndrome: Parents take care of their child from her birth. He wants his child to be healthy and make a progress. But many times the body gives birth to diseases that are challenged to treat. Excessive long hand, red mark on the skin or spinal curvature, these are no symptoms. This is a birth problem known as Cloves syndrome. Cloves syndrome is a rare disease that occurs at birth. This is the reason that to make people aware of this problem, the cloth syndrome Awareness Day is celebrated every year. What is this syndrome and what is the way to deal with it, let’s know about it.

What is the cloth syndrome

Kalows syndrome, whose full name is congenital lipomatous overgrowth, vascular malformations, epidermal nevi and spinal/skeletal anomals and/or scoliosis. This is a rare congenital condition. Cloves syndrome is a rare disease that occurs at birth. Many times it is considered other syndromes such as klippel-trnaunay or proteus syndrome, which can delay diagnosis. This is caused by mutations in Pik3CA genes, which promotes abnormal growth in body cells. This mutation is not hereditary, so it does not go from parents to the child.

Clavic syndrome

The Cloves syndrome is a non-hydrity disorder caused by a gene called Pik3CA. In this situation, cells may increase or decrease uncontrollably. In some cases environmental factors can also cause trigger of this syndrome.

Major symptoms of cloth syndrome

Hyperplasia of fat: At birth, soft fatty lumps may appear on the back, waist, abdomen or buttocks. They may have red-pink marks on the skin above them.

Abnormalities: The veins spread over the chest, hands or feet can make blood clots, which can be dangerous for the lungs. Limfetic abnormalities that can occur in the stomach, chest or organs.

Abnormalities of hands and feet: Large or uneven hands, legs, more distance between fingers or size of uneven organs are common.

Spinal problems: Spinal curvature, spinal pressure lumps or tedd cord can be.

Skin scars: Port-wine staine may be seen as embossed veins or brown skin.

Kidney problems: A kidney can be small or uncommon. Some children are at risk of Willms Tumor, for which ultrasound examination is necessary.

How to Dygnose to Cloves Syndrome

After birth, it is treated on the basis of physical examination and symptoms. However, its symptoms can be small, so examination from an experienced specialist is necessary.

– It can be initially investigated according to the family history.

-Get imaging tests like MRI, CT scan, ultrasound and X-ray.

– To confirm Pik3CA gene mutation, get molecular genetic test.

Clevs syndrome treatment

There is no cure for the cloth syndrome, but peliative care is given to prevent symptoms and improve the quality of life.

Sclerotherapy: This non-surgical process reduces the size of visual disorder.

Embolasis: This minimum invasive process controls blood vigningly disorder.

Surgery: Debalking surgery can be performed to remove hyperplastic tissue or lumps.

IVC Filter: This device prevents blood clots from reaching the lungs.

Take these precautions

– A team of experienced experts is required for the management of Cloves syndrome.

-Parents should monitor the symptoms of the child and conduct regular checks.

– Right diagnosis and timely treatment can improve the life quality of the child.