The influence of Mother Nature is limitless, sometimes even in unexpected manifestations and forms. No matter how fast medicine develops, all the same, some manifestations in the human body are so incomprehensible and mysterious that they confuse medical scientists. Who has not felt the most common disease like a runny nose… But there are people who are born with abnormalities or acquire pathologies that cannot be treated. It is impossible to treat many genetic diseases due to the unknown source of the disease – these are rare human diseases.
The editorial staff of estet-portal.com will talk about the rarest human diseases.
Which rare human diseases occur:
Progeria is a disease that causes rapid aging of the body (all systems and organs). It can be of two types: adult type – progeria Werner and children's type - Hutchinson-Gilford. The black race of people does not suffer from such a disease, only "white" ones are affected. children. Only 80 cases of this disease have been identified on earth. The progression of the disease is accompanied by complete alopecia, the disappearance of subcutaneous fat, cyanosis of the skin. This disease cannot be cured, and for a small person it is sad. Children die by the age of 13, being outwardly old people. Sometimes at birth, the baby's body does not show that progeria has already begun, but at 2 or 3 years old, the first signs let you know that the aging process has begun.
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Alien Hand Syndrome is a terrible disease that takes away control of a limb. Sometimes this disease is confused in religion and it is believed that a person is possessed by a demon. In fact, this disease is a neuropsychiatric pathology. The human hand is not completely subordinate to the brain and can perform the opposite actions that another limb performs. "Naughty" the hand can touch objects, the body, perform actions without instructions from the brain, while it can even injure a person, choke, cut, pinch, beat. Often these seizures are accompanied by epilepsy. The disease is associated with disorders in the brain, but is not treatable.
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Autobrewery or Stray Cat Syndrome manifests itself in the body in chemical reactions: the inability to break down sugar into simple carbohydrates, so the fermentation process in the body does not end, a person is always drunk. All food and drinks are converted into alcohol. This pathology can manifest itself in both men and women. There are 13 cases of deviations in the world, and these are really rare human diseases that amaze with their mystery.
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Hereditary sensory neuropathy – it is a non-perception of pain, that is, a person does not feel pain in the limbs. Only two people out of a million can manifest such a pathology. A person does not feel pain or a change in temperature in the arms and legs. Therefore, when any process occurs in the limbs, the person cannot recognize the disease due to the absence of pain syndrome.
Hypertrichosis or Werewolf Syndrome – a person is covered with hair from head to toe. Such a disease can develop after receiving a traumatic brain injury, taking hormonal drugs in large quantities or an overdose, as well as anorexia nervosa. Women are most susceptible to this disease, but it can also occur in men. There is a family in Mexico where all male members are affected by the syndrome.
Methemoglobinemia manifests itself as a pathology of blood color. Everyone is used to the fact that the blood is red, but sometimes the blood becomes blue, blue, purple or brown. Sometimes such a disease can manifest itself after the treatment of a runny nose with silver drops, which provokes the acquisition of a blue skin color. Such a pathology does not entail serious abnormalities, pain or organ dysfunction.
Zombie Syndrome is classified as a type of paranoid-depressive schizophrenia. The patient believes that he fell ill with a serious illness or died, and his soul wanders around the world. Sometimes even relatives or close people fail to convince that a person is alive and well.
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Stone Man Syndrome or progressive fibrodysplasia (Munheimer's disease) develops due to an unspecified gene mutation. In the human body, the growth of bones and the ossification of matter are actively taking place. In world practice, there are 800 cases of a disease called second skeleton disease. So far, doctors have not been able to identify which gene gives such a pathology. Therefore, nothing but anesthesia can be prescribed to a person.
Gastroschisis – This is a disease of infants, manifested by the prolapse of the abdominal organs through the lower cleft. Today, children born with such a defect can be saved, which was previously impossible. With timely first aid and the latest developments in surgery, nine out of ten children can be saved from such an ailment.
Congenital (congenital) myotonia is also called goat syncope. The cause of this disease is a genetic abnormality. When the work of skeletal muscles is disrupted due to gene mutation, contractions and relaxation of muscle tissue occur. Doctors recommend slow exercise for people with this condition to relax the muscles.
Most often, rare human diseases occur due to a mutation of the genetic system, some of the secrets of which have not yet been disclosed.
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