Results 1 to 10 of about 2,038 (156)
Glanzmann thrombasthenia [PDF]
Orphanet Journal of Rare Diseases, 2006 Glanzmann thrombasthenia (GT) is a rare autosomal recessive bleeding syndrome affecting the megakaryocyte lineage and characterized by lack of platelet aggregation.
Nurden Alan T
doaj +3 more sources
GLANZMANNS THROMBASTHENIA [PDF]
Basrah Journal of Surgery, 2009 Tolosa-Hunt syndrome (THS) has been described as a painful, unilateral, partial or total ophthalmoplegia caused by a nonspecific granulomatous process in the cavernous sinus, the superior orbital fissure, or the orbital apex.
ZUHAIR AL-BARAZANCHImad
doaj +3 more sources
Hemorrhagic cholecystitis afflicted with glanzmann thrombasthenia patient [PDF]
Journal of Family Medicine and Primary CareHemorrhagic 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.
May AlMoshary
doaj +2 more sources
Inherited Platelet Disorders During Pregnancy and Delivery: Overview of Management Strategies and Emerging Therapeutic Considerations [PDF]
Hematology ReportsInherited 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 +2 more sources
Glanzmann thrombasthenia—A not so rare platelet function disorder in Pakistan
Global Pediatrics, 2022 Objectives: To determine the prevalence, clinical manifestations and laboratory findings of Pakistani Glanzmann Thrombasthenia patients and to assess the treatment received by these patients. Materials and Method: This cross-sectional study examined 2542
Rafia Mahmood +5 more
doaj +1 more source
European Medical Journal Hematology, 2021 This case study deals with a 32-year-old Indian male patient who presented with a traumatic head injury in the hospital, experienced uncontrolled bleeding after conducting surgery, and was eventually diagnosed with Glanzmann thrombasthenia.
Vishal Chakati +3 more
doaj +1 more source
Revista Chilena de Obstetricia y Ginecología, 2022 Objetivo: Reportar el caso de una paciente con trombastenia de Glanzmann que recibe manejo con transfusión de plaquetas con factor VII activado y realizar una revisión de la literatura referente al tratamiento y el pronóstico de esta patología durante la
Brandon A. Muñoz-Vargas +5 more
doaj +1 more source
Indian Journal of Dental Research, 2022 The Rationale: Glanzmann thrombasthenia is a rare platelet disorder affecting 0.0001% of the population. Dentists may often be unaware of this condition, and manipulation of soft tissue can lead to grave consequences, which may even result in fatality ...
Lalitha S Jairam, Sunil Babu Kotha
doaj +1 more source
Haematologica, 2015 Standard treatment for Glanzmann thrombasthenia is platelet transfusion. Recombinant activated factor VII has been shown to be successful in patients with Glanzmann thrombasthenia with platelet antibodies or who are refractory to platelet transfusions ...
Giovanni Di Minno +5 more
doaj +1 more source
Haematologica, 2015 Standard treatment for Glanzmann thrombasthenia, a severe inherited bleeding disorder, is platelet transfusion. Recombinant factor VIIa is reported to be effective in Glanzmann thrombasthenia with platelet antibodies and/or refractoriness to platelet ...
Man-Chiu Poon +5 more
doaj +1 more source