Mikulicz Disease

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Mikulich (synonym Mikulich, Coolidzha, Kulika, Kridchbach-Mikulichka) (ICD 10 F79.4, F78.5) is a rare autosomal recessive genetic disease. All people have a defective gene, but so far its encoding protein has not been found

The problem with this disease is that there are few clinics and doctors in the country who understand its entire spectrum. Which leads to inaction due to an insufficient number of specialists and, as a consequence, insufficient patient research. It is also not known what connection may exist with the birth of a child, the detection of the disease in newborns, or what the child becomes ill with after a blood transfusion from siblings.