Inherited Giant Platelet Disorders
Open Access
- 1 February 2000
- journal article
- review article
- Published by Oxford University Press (OUP) in American Journal of Clinical Pathology
- Vol. 113 (2) , 176-190
- https://doi.org/10.1309/fc4h-lm5v-vcw8-dnju
Abstract
Inherited giant platelet disorders are extremely rare. The aim of this article is to review the clinical and laboratory features of this heterogeneouKeywords
This publication has 73 references indexed in Scilit:
- A Novel Hereditary MacrothrombocytopeniaJournal of Pediatric Hematology/Oncology, 1995
- May-Hegglin anomaly: A rare cause of thrombocytopeniaEuropean Journal of Pediatrics, 1992
- Prenatal Diagnosis and Obstetrical Management of May-Hegglin Anomaly: A Case ReportFetal Diagnosis and Therapy, 1992
- Thrombospondin binds normally to glycoprotein IIIb deficient plateletsBiochemical and Biophysical Research Communications, 1991
- Sebastian platelet syndromeAnnals of Hematology, 1991
- Sebastian platelet syndrome: A new variant of hereditary macrothrombocytopenia with leukocyte inclusionsAnnals of Hematology, 1990
- Familial case of may‐hegglin anomaly associated with familial spastic paraplegiaAmerican Journal of Hematology, 1990
- Gray platelet syndrome. Demonstration of alpha granule membranes that can fuse with the cell surface.Journal of Clinical Investigation, 1987
- Isolation of the thrombospondin membrane receptor.Journal of Clinical Investigation, 1987
- Severe hemorrhage in a patient with gray platelet syndromeThe Journal of Pediatrics, 1986