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ISTH 2020 Congress

Hemophilia and Rare Bleeding Disorders » Rare Bleeding Disorders

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    • Hemophilia and Rare Bleeding Disorders
      • Rare Bleeding Disorders

Abstract Number: PB1186

A Bypass Surgery with Congenital Factor 5 and Factor 8 Deficiency

V. Okan, H.H. Şahin, D.M. Akkurd

Abstract Number: PB1196

A Digestive Hemorrhage Like No Other

Y. Cherif, S. Hamrouni, M. Mrouki, S. Derbel, F. Ben Dahmen, M. Abdallah

Abstract Number: PB1177

Achenbach Syndrome in a 19 Year-Old Girl: A Clinical Case

D.O.W. Rodrigues1, N.N.S. Magalhaes2, O.F. Santos3, L.O.W. Rodrigues4

Abstract Number: PB1199

Afibrinogenemia: Identification of a New Mutation in FGB

E. Chinni1, G.L. Tiscia1, G. Favuzzi1, B. Bruschi2, P. Coccia2, I. D'Alba2, S. Gobbi2, V. Petroni2, P. Pierani2, F. Cappucci1, L. Fischetti1, P. Vergura1, G. Vecchione1, A. De Laurenzo1, D. Colaizzo1, E. Grandone1

Abstract Number: OC 09.2

An International Multicenter Study of Bevacizumab for Bleeding in Hereditary Hemorrhagic Telangiectasia (The InHIBIT-Bleed Study)

H. Al-Samkari1,2, R. Kasthuri3, J. Parambil4, H. Albitar5, Y. Almodallal6, C. Vazquez7, M. Serra7, S. Dupuis-Girod8, C. Wilsen9, J. McWilliams9, E. Fountain10, J. Gossage10, C. Weiss11, M. Latif11, A. Issachar12, M. Mei-Zahav13, M. Meek14, M. Conrad15, D. Kuter1,2, V. Iyer16

Abstract Number: PB1206

An Italian Survey on the Real-world Use of rFXIII (Catridecacog) in Patients with Factor XIII Deficiency

E. Zanon1, S. Pasca1, G. Sottilotta2, A.C. Molinari3, L. Banov3, A. Ferretti4, P. Di Gregorio5, B. Pollio6, S.M. Siboni7, R. Palla7, L. Spiezia8, M. Pizzuti9, L.D. Notarangelo10, P. Simioni11

Abstract Number: PB1179

Blocking Tissue Factor Pathway Inhibitor (TFPI) Function Has a Therapeutic Benefit in Murine Models of Factor Deficiencies

L. Ivanciu1,2, J.R. Crosby3, A.S. Revenko3, R.J. Davidson1, R.M. Camire1,2

Abstract Number: PB1195

Characterization and Management of Patients with Mild or Moderate Hereditary Factor X Deficiency: A Retrospective Chart Review

S. Acharya1, C. Sabo2, M. Chitlur3

Abstract Number: PB1171

Clinical Characteristics of Patients with Rare Bleeding Disorders: Real-Life Data from the Netherlands (RBiN Study)

J.L. Saes1,2, M.J.A. Verhagen1,2, K. Meijer3, M.H. Cnossen4, R.E.G. Schutgens5, M. Peters6, L. Nieuwenhuizen2,7, F.J.M. van der Meer8, I.C. Kruis9, W.L. van Heerde2,10,11, S.E.M. Schols1,2, RBiN Study Group

Abstract Number: PB1182

Collagen Turnover and Plasma Ascorbic Acid Levels in Patients Suspected of Inherited Bleeding Disorders Harboring Variants in Collagen-related Genes

M. Fager Ferrari1, E. Zetterberg1, M. Rossing2, T. Manon-Jensen3, M. Pehrsson3, M. Karsdal3, J. Lykkesfeldt4, E. Leinoe5

Abstract Number: PB1191

Combined Factor Deficiencies Rare among the Rare Bleeding Disorders among Pediatric Population, Seven Years Experience in a Tertiary Care Center of Lahore, Pakistan

T. Fateen, N. Mazhar, N. Saqlain, N. Ahmed

Abstract Number: PB1208

Comparative Analysis of Three Custom Gene Panels Based on Next Generation Sequencing for Diagnostic of Inherited Coagulation Bleeding Disorders

N. Borràs1, I. Corrales2, L. Ramírez2, N. Comes2, F. Vidal3

Abstract Number: PB1198

Congenital Afibrinogenemia. Report of a Case in the Children´S Hospital of Mexico Federico Gomez

J.F. Mariano González1, A.M. Moreno González2

Abstract Number: PB1190

Congenital Combined Bleeding Disorders, a Study on a Large Number of Iranian Patients

M.R. Baghaipour1, S. Tabibian1,2, F. Ala1, M. Jazebi1, G.R. Bahoush1,3, S.E. Ahmadi2, N. Baghaipour4

Abstract Number: PB1170

Economic Burden Associated with Vaso-Occlusive Crisis Management in Patients with Sickle Cell Disease

A. Oladapo1, E. Swallow2, A. Briggs2, M.L. Zichlin2, B. Mellgård1

Abstract Number: PB1176

Efficacy and Safety of Fibrinogen Concentrate for On-Demand Treatment of Acute Bleeding and Surgical Prophylaxis in Pediatric Patients with Congenital Fibrinogen Deficiency: Results from the FORMA-04 Study

S.D. Lohade1, F. D'Souza2, G.S. Latha3, C. Khayat4, O. Zekavat5, B.A. Schwartz6, I. Kruzhkova7, C. Solomon7, S. Knaub7, F. Peyvandi8

Abstract Number: PB1175

Evaluation of the Potential Utility of the Total Thrombus-Formation Analysis System (T-TAS) in Comparison to the Platelet Function Analyzer (PFA) in Subjects with Primary Hemostatic Defects

J. Charpy1, N. Benattar2, P.-E. Chaghouri1, S.-M. Castet3, Y. Huguenin3, C. James1, M. Fiore4

Abstract Number: PB1213

Evaluation of the Skeletal Lesions in the Lebanese Patients with Afibrinogenemia

C. Djambas Khayat1, T. Younane2

Abstract Number: PB1173

Fibrin Clot Properties in Patients with Qualitative Fibrinogen Disorders: Data from the PRO-RBDD Cohort

A. Casini1,2, R. Palla3, M. Menegatti4, M. Neerman-Arbez5, P. de Moerloose6, F. Peyvandi3,4

Abstract Number: PB1203

Fibrinolytic Alterations in a Thrombomodulin-associated Coagulopathy Are Diminished by Coinheritance of a TAFI Mutation

C.S. Whyte1, S. Westbury2, R.C. Tait3, N.J. Mutch1, K. Downes4, J. Mertens5, K. Claesen5, D. Hendriks5, E. Leishman3, A. Mumford2, NIHR BioResource

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