McQuarrie Syndrome

Mac-Quarrie syndrome is a rare genetic disorder that appears early in life and can lead to serious complications. It was first described in 1975 by the American pediatrician McCurry, who studied hereditary diseases.

McQuarrie syndrome is characterized by disruption of the immune system, which leads to the development of various infections and autoimmune diseases. Patients with this syndrome often have breathing problems such as asthma, pneumonia and bronchitis. In addition, they may have digestive problems, such as stomach or intestinal ulcers.

Treatment for MacQuarrie syndrome includes the use of antibiotics, immunomodulators, and other drugs to fight infections and autoimmune diseases. Treatments to improve the functioning of the immune system may also be used.

Despite the fact that McQuarrie syndrome is a rare disease, it can lead to serious consequences for the health and life of patients. Therefore, it is important to carry out early diagnosis and treatment of this syndrome to prevent the development of complications and improve the quality of life of people suffering from it.

MacQueary syndrome is a rare multisystem genetic disease that occurs due to overexpression of the QTR9 gene group. It manifests itself in the form of malformations of the face, muscles and skull, as well as loss of intelligence. The syndrome was described by American pediatrician Jesse Goldman McQueary in 1963.