while listing these diseases itself , we prayed that shouldn't come to us...
Progeria, also known as Hutchinson-Gilford progeria syndrome (HGPS), is a rare genetic condition that causes a child's body to age fast. Most kids with progeria do not live past the age of 13. The disease affects both sexes and all races equally. It affects about 1 in every 4 million births worldwide. For more information: https://en.wikipedia.org/wiki/Progeria
Ehlers-Danlos syndrome (EDS) is a collection of inherited conditions that fit into a larger group, known as heritable disorders of connective tissue. Connective tissues provide support in skin, tendons, ligaments, blood vessels, internal organs and bones. For more information: https://en.wikipedia.org/wiki/Ehlers%E2%80%93Danlos_syndrome
Harlequin ichthyosis is a severe genetic disorder that mainly affects the skin. Infants with this condition are born with very hard, thick skin covering most of their bodies. The skin forms large, diamond-shaped plates that are separated by deep cracks (fissures). For more information: https://en.wikipedia.org/wiki/Harlequin-type_ichthyosis
Hypertrichosis (also called Ambras syndrome)
is an abnormal amount of hair growth over the body; extensive cases of
hypertrichosis have informally been called werewolf
syndrome, because the appearance is similar to the mythical werewolf.
For more information: https://en.wikipedia.org/wiki/Hypertrichosis
Epidermodysplasia verruciformis is an extremely rare disorder that makes people prone to widespread human papillomavirus (HPV) infection. This infection causes scaly macules and papules (cutaneous squamous cell carcinomas) to grow on the hands, feet, and even face. For more information: https://en.wikipedia.org/wiki/Epidermodysplasia_verruciformis
Hydrocephalus is a brain condition that gets its name from the Greek word for water (meaning "hydro") and head (meaning "cephalus"). It occurs when cerebral spinal fluid (CSF) � the clear, water-like fluid that surrounds and cushions the brain and spinal cord � is unable to drain from the brain. For more information: https://en.wikipedia.org/wiki/Hydrocephalus
It is also known as Butterfly Disease, it is an inherited connective tissue disease causing blisters in the skin and mucosal membranes. The cause of this disorder is genetic mutation and for the whole life, you�ll be treating the wounds that refuse to heal. This disease may happen in 1 out of 50,000 people. Under this disease is the case of Baby Easton. The said baby was born with Epidermolysis Bullosa on August 23, 2012 which is a severely painful, incurable rare genetic skin disease. According to a certain research, skins on most of his limbs were missing, covered in scary, deep red, open wounds. For more information: https://en.wikipedia.org/wiki/Epidermolysis_bullosa
A rare hereditary defect of the enzyme system that repairs DNA after damage from ultraviolet rays, resulting in extreme sensitivity to sunlight and a tendency to develop skin cancer. For more information: https://en.wikipedia.org/wiki/Xeroderma_pigmentosum
Myiasis is infection with a fly larva, usually occurring in tropical and subtropical areas. There are several ways for flies to transmit their larvae to people. Some flies attach their eggs to mosquitoes and wait for mosquitoes to bite people. Their larvae then enter these bites. Other flies' larvae burrow into skin. For more information : https://en.wikipedia.org/wiki/Myiasis
Necrotizing fasciitis (neck-ro-tie-zing Fas-e-i-tis) is a serious bacterial skin infection that spreads quickly and kills the body's soft tissue. (Necrotizing means "causing the death of tissues.") Accurate diagnosis, prompt treatment with antibiotics through a vein, and surgery are important to stopping this infection that can become life-threatening in a very short amount of time. Commonly called a "flesh-eating infection" by the media, this rare disease can be caused by more than one type of bacteria. For more information : https://en.wikipedia.org/wiki/Necrotizing_fasciitis