Robinow Syndrome is a genetic disorder that has two forms and can cause multiple and severe defects is those who are inflicted with it. Read on to …
Continue ReadingEctodermal dysplasia (ED) is a group of inheritable disorders causing the hair, teeth, nails and glands to develop and function abnormally. The …
Continue ReadingAlfi’s syndrome, or the 9p minus syndrome, is a very rare chromosomal disorder that causes mental and physical disabilities. This article …
Continue ReadingRussell Silver syndrome, or RSS, is a condition where children show symptoms such as low body weight, asymmetry, and growth retardation. A defect in a …
Continue ReadingFamilial Adenomatous Polyposis is an inherited disorder that often results in colon cancer. In this article, the symptoms, genetics, prevalence, …
Continue ReadingThe genetic disorder commonly referred to as Pallister-Hall Syndrome can cause severely abnormal growth and development defects in people who have a …
Continue ReadingXeroderma pigmentosum is an inherited skin and eye disorder that leaves its sufferers prone to severe sunburn, skin damage and cancer, among other …
Continue ReadingWAGR syndrome is a rare genetic disorder that causes four distinct symptoms. Learn more about the genetics, prevalence, prognosis, diagnosis and …
Continue ReadingJoubert syndrome, a rare genetic disorder, primarily affects the development of the brain. This article briefly discusses the symptoms, genetics, …
Continue ReadingMobius syndrome is a rare genetic disease, primarily characterized by the inability to use the facial muscles. Even though there is no cure at …
Continue ReadingAbout 1 in 40,000 people have Pompe disease, which is a genetic condition that leaves muscles severely weakened and causes certain death if left …
Continue ReadingEpidermolysis bullosa simplex is a rare inherited disease in which the skin readily blisters in response to minor injury or friction. Read all about …
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