- Proteus syndrome - Wikipedia
Proteus syndrome is an overgrowth disorder caused by a rare genetic mosaicism A genetic mutation during embryonic development gives rise to overgrowth in a subset of the individual's cells
- Proteus Syndrome: Symptoms Causes - Cleveland Clinic
Proteus syndrome is a very rare genetic disease characterized by the overgrowth of certain parts of your body The condition can affect your bones, tissues, organs and skin, and it causes portions of your body to grow asymmetrically
- Proteus Syndrome: One of the Rarest Diseases in the World - WebMD
Proteus syndrome is one of the rarest genetic conditions in the world The syndrome causes abnormal overgrowth in certain parts of the body It is commonly called the Elephant Man disease This
- Proteus syndrome | About the Disease | GARD - Genetic and Rare Diseases . . .
Some people with Proteus syndrome have neurological abnormalities, including intellectual disability, seizures, and vision loss, as well as distinctive facial features Proteus syndrome is caused by a change in the AKT1 gene It is not inherited, but occurs as a random genetic change in a body cell in a developing baby (fetus) early in pregnancy
- Proteus Syndrome - GeneReviews® - NCBI Bookshelf
Proteus syndrome (PS) is characterized by progressive segmental or patchy overgrowth most commonly affecting the skeleton, skin, adipose, and central nervous systems
- Proteus syndrome: MedlinePlus Genetics
Proteus syndrome is a rare condition characterized by overgrowth of the bones, skin, and other tissues Explore symptoms, inheritance, genetics of this condition
- Proteus Syndrome: Symptoms, Treatment, Outlook, and More
Proteus syndrome, sometimes called Elephant Man’s disease, is a rare congenital disorder We’ll explain what causes it, and how it’s diagnosed
- Proteus Syndrome - Symptoms, Causes, Treatment | NORD
Learn about Proteus Syndrome, including symptoms, causes, and treatments If you or a loved one is affected by this condition, visit NORD to find resources
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