Results 91 to 100 of about 3,107 (209)

Disease Burden in Patients with Glanzmann’s Thrombasthenia: Perspectives from the Glanzmann’s Thrombasthenia Patient/Caregiver Questionnaire

Journal of Blood Medicine, 2020
Alexander Duncan,1 Angela Kellum,2 Skye Peltier,3 David L Cooper,4 Hossam Saad4 1Department of Pathology & Laboratory Medicine, Emory University School of Medicine, Atlanta, GA, USA; 2Louisiana Center for Bleeding and Clotting Disorders, Tulane ...
Duncan A, Kellum A, Peltier S, Cooper DL, Saad H   +4 more
doaj  

Management of Pregnancy in a Chilean Patient with Congenital Deficiency of Factor VII and Glanzmann’s Thrombasthenia Variant

Case Reports in Obstetrics and Gynecology, 2014
Patients with inherited bleeding disorders are rare in obstetric practice but present with prolonged bleeding even after minor invasive procedures. They require a combined approach with obstetric and hematological management of each case, including the ...
Nigel P. Murray, Claudio Garcia, Javier Ilabaca, Nestor Lagos   +3 more
doaj   +1 more source

Sheehan's Syndrome Associated with Glanzmann's Thrombasthenia: Case Report and Literatur Review

, 2008
Objectives: We aimed to present a case of Sheehan's syndrome associated with Glanzmann's ...
Bayraktaroglu, T., N. Colak, Colak N, Colak, N., Meliha Nalcaci, T. Bayraktaroglu, Yenerel, Mustafa Nuri, Taner Bayraktaroglu, M. Nalcaci, M. Yenerel, Mustafa Nuri Yenerel, Nalcaci, M.   +11 more
core   +1 more source

Association of xeroderma pigmentosum with thrombasthenia

The Turkish Journal of Pediatrics, 1996
Xeroderma pigmentosum (XP) is an autosomal recessive disorder characterized by severe sun-sensitivity, early skin cancers and abnormal DNA repair. XP has a worldwide distribution with an approximate frequency of 1/250,000.
A Hasanoğlu, K Gücüyener, L Tümer, T Gürsel   +3 more
doaj  

Periodontal Management of Glanzmann's Thrombasthenia: Report of 3 Cases

, 1996
GLANZMANN'S THROMBASTHENIA WAS REPORTED and described as a bleeding diathesis seen in children and characterized by diminished clot retraction. It is an autosomal recessive bleeding disorder.
Tanju Atamer, Alpdoǧan Kantorci, Cebeci, I, Kantarci, A, Tuncer, O, Özen Tuncer, Irfan Cebeci, Erhan Firatli, Atamer, T, Firatli, E   +9 more
core   +1 more source

Feminizing genitoplasty in a young girl with glanzmann\u27s thrombasthenia-management of haemostasis [PDF]

, 2020
We report peri- and post-operative management of haemostasis in a 11-year old girl with Glanzmann Thrombasthenia (GT) who had feminizing genitoplasty for genital ambiguity due to Congenital Adrenal Hyperplasia (CAH-21 Hydroxylase deficiency).
Turk, Kashaf Khalid, Nazir, Zafar
core  

Molecular characterization of Glanzmann's thrombasthenia in Iran: Identification of three novel mutations

, 2017
Quantitative and/or qualitative defects of the platelet membrane glycoprotein IIb/IIIa complex lead to the clinical entity of Glanzmann's thrombasthenia.
Vahidi, R., Abolghasemi, H., Faranoush, M., Ala, F., Farsinejad, A., Kazemi, A., Kazemzadeh, S.   +6 more
core  

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

Case 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, Mohadese Poorpouneh, Samira Rafiee   +2 more
doaj   +1 more source

Surgical resection of a sphenoid wing meningioma in a patient with Glanzmann thrombasthenia.

, 2011
peer reviewedGlanzmann thrombasthenia (GT) is a rare autosomal recessive disorder characterized by a deficiency or functional defect of platelet glycoprotein (GP) IIb/IIIa.
WERTZ, Damien, LENELLE, Jacques, Boveroux, Pierre, FRANSSEN, Colette, PETERS, Pierre   +4 more
core   +1 more source

A novel Ser123Pro substitution in the MIDAS domain of integrin 3 associated with variant Glanzmann's thrombasthenia in an Indian patient

Haematologica, 2004
We report a novel 465T-->C (S123P) mutation in exon 3 of the GPIIIalpha gene in a patient with type III or variant Glanzmann's thrombasthenia (GT).
S Nair, K Ghosh, S Shetty, D Mohanty
doaj