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Research by matthew warman, md, director of boston children’s orthopedic research laboratories, and pathologist kyle kurek, md, has revealed that cloves is caused by mutations in a gene called pik3ca Cloves stands for c ongenital l ipomatous assymetric o vergrowth, v ascular malformations, e pidermal nevi and s keletal and spinal anomalies. These mutations arise spontaneously in the womb, while a baby is developing.
Cloves syndrome is a rare condition that is primarily characterized by congenital overgrowth of fatty tissue This disorder causes abnormalities in blood vessels, skin, spine, joints and bones Malformations of the vascular system (the vessels that carry blood and lymph throughout the body)
And spinal or skeletal abnormalities
Other signs and symptoms may include disproportionate fat distribution, overgrowth of the extremities (arms and legs), skin. Cloves syndrome is a rare overgrowth syndrome with complex vascular anomalies Cloves syndrome is a very rare genetic disorder that causes vascular, skin, spinal, and bone or joint abnormalities. A new diagnosis of a rare syndrome like cloves syndrome can be a challenging time that may cause anxiety and stress for patients and families
We believe that connecting to others is an important component of a new diagnosis and may help to put some of the uncertainty and concern into perspective. Learn about cloves syndrome, including symptoms, causes, and treatments If you or a loved one is affected by this condition, visit nord to find resources and Cloves syndrome symptoms, causes, and treatment cloves syndrome, also known as congenital lipomatous overgrowth, vascular malformations, epidermal nevi, and spinal/skeletal anomalies and/or scoliosis (cloves) syndrome, is a rare genetic disorder that affects various parts of the body
It is caused by mutations in specific genes.
Cloves syndrome is an extremely rare condition It is a disorder that is present at birth (congenital)
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