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-Samkari^1,2, 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. Kuter^1,2, 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. Ivanciu^1,2, J.R. Crosby³, A.S. Revenko³, R.J. Davidson¹, R.M. Camire^1,2

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. Saes^1,2, M.J.A. Verhagen^1,2, K. Meijer³, M.H. Cnossen⁴, R.E.G. Schutgens⁵, M. Peters⁶, L. Nieuwenhuizen^2,7, F.J.M. van der Meer⁸, I.C. Kruis⁹, W.L. van Heerde^2,10,11, S.E.M. Schols^1,2, 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. Tabibian^1,2, F. Ala¹, M. Jazebi¹, G.R. Bahoush^1,3, 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. Casini^1,2, R. Palla³, M. Menegatti⁴, M. Neerman-Arbez⁵, P. de Moerloose⁶, F. Peyvandi^3,4

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