Thrombocytopathy
I. А. Demina
1
, M. A. Kumskova
1
, M. A. Panteleev
1–4
1
Federal Research Center of Pediatric Hematology, Oncology and Immunology named after Dmitriy Rogachev,
Ministry of Health of Russia; 1 Samory Mashela St., Moscow, 117198, Russia;
2
Hematological Research Center, Ministry of Health of Russia; 4a Novo-Zykovskiy Pr-d, Moscow, 125167, Russia;
3
Theoretical Problems Center of Physical and Chemical Pharmacology, Russian Academy of Sciences;
38A, Bldg. 1, Leninskiy Prosp., Moscow, 119991, Russia;
4
M.V. Lomonosov Moscow State University; 1, Bldg. 8 Leninskie Gory St., Moscow, 119234, Russia
The article is devoted to general issues of classification and differential diagnosis of thrombocytopathy. Features of pathogenesis, clinical
course and diagnosis of certain rare inherited thrombocytopathies are highlighted. Particular attention is paid to the formation of the molecu-
lar basis of these diseases. The basic genetic mutations associated with a number of thrombocytopathies are given.
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