- Young Children Are Unintentionally Given Wrong Medications Frequently
- Male And Female Heart Reacts Differently To Mental Stress
- Cells From Placenta Are Safe For Multiple Sclerosis Treatment
- New Knowledge Of Bladder Cancer Causing Genes Helps In Targeted Treatment
- Immunity In Long-term May Altered With Antibiotics In Early Life
Top 10 Rarest Diseases in The World
Rare diseases are hereditary in nature and may only affect a small percentage than the common disease that can found in some people.
Here is a list of 10 diseases that rarely affect people:
Water allergy: Water allergy disease is very rare and is affected only 30 individuals till date. This kind of disease causes skin to become unbearably itchy and burning after exposure to water. These symptoms will last anywhere from ten minutes to several hours.
Microcephaly: Microcephaly is extremely rare condition of the nervous system that is visible immediately at birth or even before. It affects 1 in every 666,666 in the U.S. Because of this disease, patient’s physical development is significantly unnatural as well as mental development is also delayed.
Argyria (blue skin) : Argyria is rare disease which is characterized by a blue or gray discoloration on the skin. It is due to an extreme exposure from silver or an intake of sliver salts, which are found in particular prescription medications. The main symptoms include headaches, weakness, dizziness, breathing difficulties and psychological changes.
Werewolf Syndrome: Werewolf is rare genetic disorder that cause excessive amount of hair growth on the body where hair will not supposed to develop. The hair typically grows on face, hands and arms. In medical term, it is referred as hypertrichosis or ambras syndrome.
Human Pappiloma Virus: Human pappiloma virus is also another rare skin disorder which is genetic in nature. It is a result of some immunity deficiency which in turn causes a typical skin disorder.
They are found all over the body, but sometimes it can be targeted to the parts of the body which often are exposed to the sun.
Hutchinson-gilfordprogeria: This genetic disease is more often known as progeria. It affects because of a new mutation characterized by the dramatic and rapid appearance of aging starting in childhood.
This disorder affects one in 8 million people all over the world. The usual life time of the people who are suffering from this particular disease is 13 years while some others are able to survive until their early twenties.
Cutaneous horns: A cutaneous horn is also uncommon hereditary condition. It grows on human feet and hands. This happens to adults, particularly those who are frequently exposed in the sun.
Fields’ disease: Field’s disease is also one of the rarest neuromuscular diseases in the world. With the cause of this disease, the muscles of the body gradually begin deteriorating and additional limit the body movements. This disorder affects only girls and till now it is restricted the lives of so many girls to wheelchairs.
Fibrodysplasia Ossificans Progressiva: This can be a rare disorder in which muscle tissues as well as connective tissues like ligaments and tendons are slowly substituted by bones and develop bones outside the skeleton that constrains your normal movements.
Moebius syndrome: It is a neurological disorder where the cranial nerves are damaged. It includes the eye and face muscles that leads to partial and total facial paralysis. The main symptoms of this disorder are lack of facial expressions, crossed eyes, inability to smile and to move the head.