Inherited thrombocytopenias are a heterogeneous group of rare diseases characterized by reduced numbers of blood platelets. The clinical spectrum ranges from severe syndromal forms with multiorgan involvement and severe bleeding to mild conditions that may remain undetected. In most cases, defects have been described in genes coding for membrane glycoproteins, cytoskeletal components, intracellular signaling pathways, and transcription factors. However, the pathophysiologic mechanisms remain elusive in a number of diseases. This review describes pathophysiologic, clinical, and diagnostic aspects of inherited thrombocytopenias.

Erblich bedingte Thrombozytopenien

BALDUINI, CARLO;
2006-01-01

Abstract

Inherited thrombocytopenias are a heterogeneous group of rare diseases characterized by reduced numbers of blood platelets. The clinical spectrum ranges from severe syndromal forms with multiorgan involvement and severe bleeding to mild conditions that may remain undetected. In most cases, defects have been described in genes coding for membrane glycoproteins, cytoskeletal components, intracellular signaling pathways, and transcription factors. However, the pathophysiologic mechanisms remain elusive in a number of diseases. This review describes pathophysiologic, clinical, and diagnostic aspects of inherited thrombocytopenias.
2006
(area 06) The General & Internal Medicine category covers resources on medical specialties such as general medicine, family medicine, internal medicine, clinical physiology, pain management medicine, geriatric medicine, military medicine, and hospital medicine.
Esperti anonimi
Tedesco
Internazionale
STAMPA
154
6
510
521
12
Bleeding diathesis; Thrombocytopathy; Thrombocytopenia; Pediatrics, Perinatology and Child Health
4
info:eu-repo/semantics/article
262
Ballmaier, M.; Balduini, Carlo; Welte, K.; Germeshausen, M.
1 Contributo su Rivista::1.1 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/1125263
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