kletig
Kletig is a rare and complex genetic disorder characterized by the absence of the ability to produce sweat. This condition is often referred to as "dry skin syndrome" or "anhidrosis." The primary cause of kletig is a mutation in the KCNJ5 gene, which encodes for a potassium channel protein. This mutation leads to a disruption in the normal functioning of sweat glands, resulting in the inability to produce sweat.
Kletig can manifest in various ways, including dry skin, excessive sweating in response to heat or emotional
The prevalence of kletig is estimated to be around 1 in 100,000 individuals. It is more commonly
Research into the underlying mechanisms of kletig and the development of potential treatments is ongoing. Understanding