Leške Syndrome

Leshkoff syndrome is a rare hereditary disease that is characterized by decreased intelligence, psychomotor impairment and other health problems. With each generation, the percentage of patients decreases due to the small population of people who suffer from this syndrome, but there are also successful cases of cure using gene therapy. Below are the main characteristics of Leshkoff syndrome:

1. Clinical manifestations Leshkoff syndrome manifests itself in the form of mild to severe mental disorders, such as mental impairment, learning difficulties, memory and thinking disorders, behavioral disorders, aggression and depression. The disease is also accompanied by chromosomal abnormalities, such as deletion of the short arm of chromosome 7, leading to intellectual impairment. The average age of onset of the syndrome is 5–7 years, although clinical signs may occur before then. Parents suffer from high levels of depression, and lack of diagnosis can lead to treatment refusal.

2. Diagnosis The disease is detected through genetic testing or DNA testing, which can identify the genetic abnormalities associated with Leshkoff syndrome. In some cases, additional tests are required, such as an MRI of the head.

_Leschke syndrome_ is a rare hereditary disease that manifests itself in the form of impaired pigmentation of the skin and mucous membranes. This disease is genetic in nature and is inherited from parents to children. Leschke syndrome is quite rare, but at the same time a serious disease that requires complex treatment and care. In this article we will look at the main