Modern medicine is developing, and now many diseases that were previously considered incurable are successfully corrected and treated. However, in the world to this day there are a number of physical and mental diseases that are difficult to treat. Many of them are extremely rare, and patients suffering from them can be counted on the fingers. HUTCHINSON’S DISEASE
Progeria, or Hutchinson's disease, is one of the
most famous rare diseases. Due to congenital genetic anomalies, the body of a small child begins to age at a tremendous rate. At the same time, his psychological development remains, as expected, at the children's level. The appearance of the child becomes characteristic of the disease when he is 2 or 3 years old. He is diagnosed with severe stunting, loss of skin elasticity, lack of hairline. Veins appear on thin and pale skin.
Progeria is twice as common in boys as in girls.
Around the world, approximately 80 people with this pathology are officially registered. Death from progeria occurs at the age of 10-13, but there are cases when patients live up to 27-30 years. In Japan, a kind of record was set when a person lived to be 45 years old and died of progressive heart failure. ARGYRIA
"Blue skin syndrome", or argyrosis, doctors had to
observe, at least in two different parts of the globe. The first case was in California resident Paul Carason. His skin took on a silvery blue color when he was 57 years old. The reason for the dramatic change in the skin was the uncontrolled use of a silver- based balm, which Paul made himself. A similar phenomenon occurred in Russia. A resident of Kazan, Valery V., once simply dripped drops into his nose, which included silver, as a result of which his hair brightened dramatically, and his skin turned silver-blue. FOREIGN LANGUAGE SYNDROME
One of the patients, American Michelle
Myers, went to bed in the evening with a terrible headache in 2015. When she woke up, she realized that she had a British accent that stayed with her for years to come. Prior to that, according to Myers, after the same severe headaches, she woke up with Irish and Australian accents, but they disappeared after a week.
This pathology is not associated with genes, but, as a
rule, with head injuries or strokes. With the disease, patients' speech is still intelligible, but they use pronunciation and intonations that are characteristic of another language. To date, only about 60 cases of the syndrome are known. Ultraviolet is dangerous not only for fictional vampires, but also for heavy people suffering from xeroderma disease. This is a hereditary disease that XERODERMA causes adverse effects of ultraviolet radiation.
The disease usually manifests itself at the age of two or
three years. Peeling, irritation, spots on the skin. With each episode of the appearance of the manifestation of light, the symptoms are aggravated. A few years later, skin atrophy, uneven pigmentation, vascular formations, cracks, and crusts are observed in places. The disease is not only the skin, but also the connective tissue. As a result, over time, the nostrils, auricles, and mouth are deformed. In the final stage of development, benign and malignant tumors arise. 2/3 of patients die before the age of 15 years. The fact that there are often no existing effective cures adds to the high level of pain and suffering endured by patients and their families.
Rare diseases not only affect the person diagnosed –
they also impact families, friends, care takers and society as a whole. The European Union considers a disease as rare when it affects less than 1 in 2,000 citizens. Rare diseases currently affect 3.5% – 5.9% of the worldwide population. Over 6,000 different rare diseases have been identified to date. 72% of rare diseases are genetic whilst others are the result of infections, allergies and environmental causes. YOU CAN'T BUY HEALTH, YOU CAN ONLY PAY FOR IT.