Gray Platelet Syndrome [syndrom šedých destiček]

topical
1
Terms

alfa-granule destiček - deficit
alfa-granule trombocytů - deficit
deficit alfa-granul trombocytů
nedostatek alfa-granul trombocytů

 

Grey Platelet Syndrome
Platelet alpha-Granule Deficiency

Persistent link   https://www.medvik.cz/link/D055652
Definition

A rare, inherited platelet disorder characterized by a selective deficiency in the number and contents of platelet alpha-granules. It is associated with THROMBOCYTOPENIA, enlarged platelets, and prolonged bleeding time.

DUI
D055652 MeSH Browser
CUI
M0519284
Previous indexing
Blood Platelet Disorders (1971-2008)
History note
2009
Public note
2009

C Diseases
C15.378.140.120 Bernard-Soulier Syndrome 9
C15.378.140.427 Gray Platelet Syndrome 1
C15.378.140.810 Thrombasthenia 7
C15.378.140.855 Thrombocytopenia 601
C15.378.140.860 Thrombocytosis 60
C15.378.140.900 von Willebrand Diseases 103
C16.320.099.056 Afibrinogenemia 39
C16.320.099.080 Bernard-Soulier Syndrome 9
C16.320.099.300 Factor V Deficiency 7
C16.320.099.310 Factor VII Deficiency 6
C16.320.099.320 Factor X Deficiency 2
C16.320.099.325 Factor XI Deficiency 12
C16.320.099.330 Factor XII Deficiency 8
C16.320.099.335 Factor XIII Deficiency 4
C16.320.099.417 Gray Platelet Syndrome 1
C16.320.099.500 Hemophilia A 688
C16.320.099.510 Hemophilia B 214
C16.320.099.515 Hermanski-Pudlak Syndrome 7
C16.320.099.550 Hypoprothrombinemias 4
C16.320.099.690 Protein C Deficiency 31
C16.320.099.820 Thrombasthenia 7
C16.320.099.920 von Willebrand Diseases 103
C16.320.099.970 Wiskott-Aldrich Syndrome 20