Results 61 to 70 of about 3,107 (209)

Spontaneous haemothorax: An uncommon presentation of Glanzmann thrombasthenia

, 2002
Glanzmann thrombasthenia is a rare hereditary qualitative platelet disorder characterized Dy a lifelong bleeding tendency due to quantitative and qualitative abnormalities of the platelet integrin αIIbβ3.
Fisgin, T., Duru, F., Yarali, N., Kara, A.   +3 more
core   +1 more source

Anesthetic experience for orthopedic surgery on a patient with Glanzmann's thrombasthenia refractory to platelet transfusion: A case report [PDF]

, 2009
Glanzmann's thrombasthenia is an autosomal recessive bleeding disorder caused by qualitative or quantitative abnormalities of the platelet glycoprotein IIb/IIIa (GP IIb/IIIa), which can lead to excessive bleeding.
신양식
core   +1 more source

Bleeding Disorders in Children With Genetic Diseases: A Narrative Review

Acta Paediatrica, Volume 115, Issue 5, Page 1015-1024, May 2026.
ABSTRACT Aim The lack of data on bleeding risk assessment in children with genetic diseases is concerning given their increased care needs and risk of haemorrhagic complications compared to the general population. Identification of haemostatic disorders is crucial for implementing preventive measures and mitigating bleeding risk.
Raphaelle Cagol, Mariam Sbeity Barakat, Marjolaine Willems, Tasnime Akbaraly, Biron‐Andreani Christine, Isabelle Diaz, Alexandre Theron   +6 more
wiley   +1 more source

National Bleeding Disorder Foundation Clinical Practice Recommendations for Laboratory Screening of Iron Deficiency With and Without Anemia in the Inherited Bleeding Disorders Population

Haemophilia, Volume 32, Issue 3, Page 646-657, May/June 2026.
ABSTRACT Introduction The National Bleeding Disorder Foundation (NBDF) Medical and Scientific Advisory Council (MASAC) was formed in 1954 and issues recommendations and advisories pertinent to the bleeding disorders community. MASAC is comprised of > 25 rotating members from different medical disciplines and lived experience experts.
Glaivy Batsuli, Magdalena D. Lewandowska, Ming Y. Lim, Kelly Tickle, Maureen K. Baldwin, Rose Bender, Jennifer Davila, Brendan Hayes, Amanda Jacobson‐Kelly, Peter Kouides, Michele P. Lambert, Shilpa Nataraj, Michelle Sholzberg, Roona Sinha, Hanny Al‐Samkari, Amy L. Dunn   +15 more
wiley   +1 more source

Glanzmann Thrombasthenia in a Newborn with Heterozygous Factor V Leiden and Heterozygous MTHFR C677T Gene Mutations

, 2019
IntroductionGlanzmann thrombasthenia is a rare congenital platelet dysfunction.Case characteristicsA 2-day-old male neonate delivered at 35 weeks' gestation was referred with extensive bruising and jaundice. His elder sibling had Glanzmann thrombasthenia,
Yilmaz, Fatma Hilal, Caliskan, Umran, Tarakci, Nuriye, Gultekin, Nazli Dilay, Tokgoz, Huseyin   +4 more
core   +1 more source

Perioperative management of a Glanzmann thrombasthenia patient undergoing off-pump coronary artery bypass graft surgery: A case report [PDF]

, 2023
Background: Glanzmann thrombasthenia is a rare bleeding disorder caused by defective platelet aggregation and characterized by mucocutaneous bleeding: recurrent untriggered episodes of epistaxis and gingival bleeding.
Bayan F. Alqtishat, Hasan Hajjaj, Ruba Salameh, Nizar Awwad   +3 more
core   +1 more source

Effects of Spectral Interfering Substances on Light Transmission Platelet Aggregation Using Infrared Based Aggregometer

Journal of Clinical Laboratory Analysis, Volume 40, Issue 2, January 2026.
This study aims to investigate the nature and extent of hemolyzed, icteric, or lipemic (HIL) interference on platelet aggregation using the TA‐8 V aggregometer (Diagnostica Stago, Asnières sur Seine) equipped with a near‐infrared light source outside the typical absorbance range of HIL.
Manal Ibrahim‐Kosta, Gaïa Zirka, Karine Carriere, Philippe Ohlmann, Marie‐Christine Alessi   +4 more
wiley   +1 more source

A patient with glanzmann's thrombasthenia for emergent abdominal surgery

, 2004
Glanzmann's thrombasthenia is a rare autosomal recessive disease characterized by potentially major mucocutaneous complications and nose bleeds. It is considered hazardous for these surgical patients to conceive, with a high risk of urgent surgery.
Erciyes, N, Bostan, Habib, Senel, AHMET CAN, Uzunlar, Halil, Eroglu, AHMET   +4 more
core   +1 more source

Hemorrhagic cholecystitis afflicted with glanzmann thrombasthenia patient. [PDF]

J Family Med Prim Care
Hemorrhagic cholecystitis is a rare and potentially life-threatening condition that requires immediate medical attention. If the gallbladder perforates, it can lead to even more severe complications.
AlMoshary M.
europepmc   +2 more sources

ITGA2B/ITGB3‐Related Macrothrombocytopenia Associated With Gain‐of‐Function Mutations in ITGA2B or ITGB3 Genes

Journal of Cellular and Molecular Medicine, Volume 30, Issue 1, January 2026.
ABSTRACT Glanzmann thrombasthenia (GT) is an inherited hemorrhagic disorder characterised by impaired platelet functions, manifested clinically as spontaneous bleeding. It is usually inherited in an autosomal recessive manner. Platelet dysfunction in patients with GT is caused by quantitative and/or qualitative deficiencies in αIIbβ3, which result from
Jiao Wu, Han Yan, Zijian Li, Yilin Zhu, Ruonan Shao, Honglei Xin, Tongyu Jia, Mengyu Ge, Lu Zhang, Suyu Jiang, Jianhua Mao, Jiansong Huang, Chao Fang, Xiaodong Xi, Xiaofeng Shi   +14 more
wiley   +1 more source