.003788 but was not found in the Tatar or Bashkir populations. The disease incidence is estimated to be 1.43 (95% CI: 0

, and autoinflammatory disease due to type I IFN. Here, we show that a dominant negative mutation in the gene encoding

Клинический случай ксероза роговицы на фоне ихтиоза кожи is presented. Clinical manifestations of change occurring in the eyes of the patient disease are outlined

researched – 89.91%, despite a good response to primary therapy, had a relapse of the disease after 7 years

Наследственные формы злокачественных новообразований молочных желез: прогноз, скрининг и профилактика. Обзор литературы programs should take into account the early age of disease manifestation, high breast density in young

Восстановление анатомического соотношения элементов анального канала путем пластики связки Паркса при геморрое IV стадииhemorrhoidal disease