Results 51 to 60 of about 1,325 (125)

Acquired Platelet Dysfunction Secondary to Myelodysplastic Neoplasm: Successful Resolution With Neoplasm‐Directed Therapy

open access: yesCase Reports in Hematology, Volume 2026, Issue 1, 2026.
Acquired platelet dysfunction has been reported as a complication of hematologic malignancies. Diagnosis and management of platelet dysfunction with a concomitant myeloid disorder can be challenging, and there is a need for real‐world experience reports to help clinicians recognize these entities and manage them accordingly. Herein, we report a case of
Amy Hockman   +5 more
wiley   +1 more source

Clinico-Demographic Trends in Inherited Bleeding Disorders: Insights from Dhaka Medical College

open access: yesHaematology Journal of Bangladesh
Background: The blood coagulation system is very delicately balanced; is maintained in a fluid state in the vasculature and rapidly clots to seal an injury.
Nahid Sultana   +9 more
doaj   +1 more source

Glanzmann thrombasthenia and its perioperative management in head trauma: A rare and challenging situation

open access: yesJournal of Neuroanaesthesiology and Critical Care, 2016
Glanzmann thrombasthenia is a rare inherited coagulation disorder, manifesting itself in early childhood as bleeding episodes. The patients with this disease may present with uncontrollable bleeding following trauma.
Neeraj Kumar   +5 more
doaj   +1 more source

Co‐inheritance of ITGA2B and TUBB1 variants in a family reveals distinct genetic contributions to platelet dysfunction

open access: yes
British Journal of Haematology, Volume 208, Issue 6, Page 2298-2303, June 2026.
Perla Bandini   +12 more
wiley   +1 more source

Inherited Platelet Disorders During Pregnancy and Delivery: Overview of Management Strategies and Emerging Therapeutic Considerations

open access: yesHematology Reports
Inherited platelet disorders (IPDs) comprise a heterogeneous group of rare conditions that present particular challenges during pregnancy, with bleeding risk increasing during labor and the immediate postpartum period. These disorders require coordinated,
Victor Zibara, Nicoletta Machin
doaj   +1 more source

Glanzmann′s thrombasthenia: A case report and review

open access: yesJournal of Indian Academy of Oral Medicine and Radiology, 2011
Glanzmann′s thrombasthenia (GT) is a rare autosomal recessive disorder and characterized by a lack of platelet aggregation due to the absence of platelet glycoprotein (GP) Ilb and Illa. Usually, the disease leads to mild hemorrhage but sometimes bleeding
Ajit D Dinkar   +2 more
doaj   +1 more source

Glanzmann thrombasthenia associated with human immunodeficiency virus-positive patient

open access: yesInternational Journal of Preventive Medicine, 2014
Glanzmann′s thrombasthenia (GT) is an autosomal recessive inherited platelet function defect characterized by normal platelet count, prolonged bleeding time and abnormal clot retraction.
Rakesh Kumar Manne   +5 more
doaj  

Profiling the Genetic and Molecular Characteristics of Glanzmann Thrombasthenia: Can It Guide Current and Future Therapies?

open access: yesJournal of Blood Medicine, 2021
Alan Nurden Institut Hospitalo-Universitaire LIRYC, Pessac, FranceCorrespondence: Alan NurdenInstitut Hospitalo-Universitaire LIRYC, Pessac, 33600, FranceEmail nurdenat@gmail.comAbstract: Glanzmann thrombasthenia (GT) is the most widely studied inherited
Nurden A
doaj  

Glanzmann's thrombasthenia: pathogenesis, diagnosis, and current and emerging treatment options

open access: yesJournal of Blood Medicine, 2015
Tia Solh,1 Ashley Botsford,2 Melhem Solh31Department of Physician Assistant Studies, Philadelphia College of Osteopathic Medicine, Suwanee, GA, USA; 2College of Health Care Sciences, Nova Southeastern University, Orlando, FL, USA; 3The Blood and Marrow ...
Solh T, Botsford A, Solh M
doaj  

Gross Hematuria Following Fetal Head Engagement in a Pregnant Woman with Glanzman Syndrome

open access: yesCase Reports in Clinical Practice
Glanzmann’s thrombasthenia (GT) is a rare genetic platelet disorder that leads to bleeding problems in affected individuals. We present a 28-year-old woman with GT who experienced a rare symptom of painless gross hematuria in the last month of pregnancy.
Azam Zafarbakhsh   +2 more
doaj   +1 more source

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