Results 51 to 60 of about 1,325 (125)
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
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 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
British Journal of Haematology, Volume 208, Issue 6, Page 2298-2303, June 2026.
Perla Bandini +12 more
wiley +1 more source
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
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
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
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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
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
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Gross Hematuria Following Fetal Head Engagement in a Pregnant Woman with Glanzman Syndrome
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

