A Brazilian woman who developed massive you die on his legs caused by a rare genetics The disorder has already undergone several surgeries to eliminate the growths, but he said it damaged his relationship and even made him lose his job. Karina Rodini, 28, said the disease had started with dark markings on her legs at the age of 2 years.

She was eventually diagnosed with neurofibromatosis, The sun has brought. The genetic disorder affects the nervous system and can cause the growth of tumors on the nerves. According to the US National Library of Medicine, the disease usually causes benign tumors, but in some cases they can become cancerous.

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Symptoms of neurofibromatosis type 1 are sometimes present at birth and may include skin changes or deformed bones. There are several types of neurofibromatosis, including type 2, which causes hearing loss, ringing in the ears and poor balance. Schwannomatosis, the rarest form of the disease, causes severe pain in patients. The diagnosis is usually based on symptoms but can be confirmed by genetic testing.

Although there is no cure for the disorder, the treatment can help control symptoms, including surgery to remove tumors, radiation and various medications.

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Rodini was operated for his case at the age of 12, about three years after the onset of tumors on his body. A 19-kilogram tumor was removed from her uterus and she would have undergone six other procedures to eliminate major growths. Rodini told the Sun that she could only get surgery every two or three years because of the magnitude of blood loss associated with the elimination of tumors.

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"Her left eye gives her poor visibility because of the disease," said Fatima Rodini, the woman's mother, at Sun. "She walks very slowly because the leg is too heavy. She also suffers from shortness of breath when she has to walk more than 20 minutes or climb the stairs. "