7 Rarest Diseases In the World
According to the Journal of Molecular Medicine, Hutchinson-Gilford Progeria Syndrome, Kuru, Fibrodysplasia Ossificans Progressiva, and Morgellons Syndrome are the rarest diseases in the world.
Rare diseases are those that affect only a small part of the total population, and researchers struggle to find causes and solutions. These diseases can be genetic and appear early in life so in this article we will talk about these rare diseases.
1- Hutchinson-Gilford Progeria Syndrome (HGPS)
The disease is rare and is present in children from the first two years of life. Babies with this syndrome usually look normal at birth.
What Are The Symptoms Of Hutchinson-Gilford Progeria Syndrome?
The following are the symptoms of Hutchinson-Gilford Progeria Syndrome (HGPS).
- Baldness
- Elongated head with small faces
- Limited body movement
- Growth retardation
- Hip migration
Is There A Cure For Hutchinson-Gilford Progeria Syndrome (HGPS)?
Lonafarnib medicine is used as a treatment for this syndrome. It improves hearing, bone structure, and blood vessels, but there is no permanent cure for Progeria.
2- Kuru
It is a very rare disease and is caused by a growing infection in the human brain. Kuru is found in the people of New Guinea who practiced a kind of cannibalism in which the brains of the dead were eaten as part of a funeral ritual.
What Are The Symptoms Of Kuru?
The signs of Kuru disease are as follows:
- Muscle jerking of the patient’s face
- Headache and pain in legs and arms
- Difficulty walking and swallowing.
Is There A Cure?
No, there is no permanent cure for Kuru.
3- Progressive Fibrodysplasia Ossificans Syndrome
Fibrodysplasia ossificans progressiva is also called Stoneman syndrome. The condition is found in the connective tissues and impairs progressive heterotopic ossification of the fingers, toes, and skeletal muscles.
What Are The Symptoms Of The Fibrodysplasia Ossificans Progressive Syndrome?
The symptoms of this syndrome are detailed below.
- Painful fibrous nodules.
- Inflamed tumors in the neck, back, and shoulders.
- Suffering from stiff joints
- Fever
Is There A Cure For Fibrodysplasia Ossificans Progressive Syndrome?
There is no permanent cure for progressive fibrodysplasia ossificans syndrome. It was only surgically removed.
4- Morgellons
It is a very rare skin disease in which dark hairs or fibers appear on the skin that cause pain and sensation.
What Are The Symptoms Of Morgellons Syndrome?
The following are the symptoms of Morgellons syndrome:
- You feel itchy, crawling, stinging, and stinging.
- Dark hair appears.
- Threads or spots under the skin
- Itching and sores
- Vision change
- Losing memory
Is There A Cure For Morgellons Syndrome?
Morgelin syndrome is treated by treating the condition. On the other hand, doctors believe that this condition is caused by mental health problems, so they prescribe psychotherapy or therapy.
5- Methemoglobinemia
Methemoglobinemia is a syndrome in which your body does not get enough oxygen and your body turns blue.
What Are The Symptoms Of Methemoglobinemia?
The following are the symptoms of methemoglobinemia.
- The color of his body changes to blue.
- You have trouble breathing.
- You feel headaches and dizziness.
- Hair lines are damaged.
- You are anemic.
- You have heart and lung disease.
Is There A Cure For Methemoglobinemia?
Yes, the doctor recommends methylene blue supplements that provide adequate oxygen to your body.
6- Microcephaly
Microcephaly syndrome is congenital. In this case, the baby’s head is smaller than normal, which means that the baby’s brain is not developing properly.
What Are The Symptoms Of Microcephaly?
The following are the symptoms of microcephaly:
- This syndrome reduces the experience of life.
- Reduce the size of the head.
- Dwarfism
- Speech delay
- Seizures and convulsions
- Low motor skills and clumsiness.
Is There A Cure For Microcephaly?
There is no cure for microcephaly syndrome, but people can generally grow and develop intelligence.
7- Parry Romberg Syndrome
Perry Romberg is a very rare condition and is more common in women than men. In this syndrome, the skin tissues soften up to the middle of the face, usually on the left side of the face.
What Are The Symptoms Of Perry Romberg Syndrome?
The following are the symptoms of Perry Romberg syndrome.
- Atrophies of the skin and connective tissue, usually on the face.
- Hair loss
- Stained
- Lack of oil on the skin
- Tissue pain
- Migraine
- Having visual abnormalities such as droopy eyelids.
- Nausea and vomiting
- Dental abnormalities
Is There A Cure For This Syndrome?
For this syndrome, the drug Immununosupper is used to help remove skin, fat, and tissue.
Outcome
If anyone in your area and in her family suffers from this syndrome, immediately see a general practitioner.
Name The Diseases For Which There Is No Permanent Cure?
- Cancer
- Dementia
- Alzheimer’s Diseases
- Diseases of the lungs, heart, kidneys and liver.
- Paralysis and other neurological disorders.
What Is The Name Of The Disease That Makes You Stone?
Living with scleroderma
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