Results 1 to 10 of about 1,408 (103)

Bernard Soulier syndrome: A case report from Pakistan. [PDF]

Clin Case Rep, 2023
Key Clinical Message Bernard Soulier Syndrome should be suspected in patients with bleeding disorder symptoms and significant family history, where consanguineous marriages are common.
Effendi I, Nadeem A, Sarfraz S, Shahid M, Farooq M, Anand A.   +5 more
europepmc   +2 more sources

Recurrent melena in a diagnosed case of Bernard Soulier syndrome. [PDF]

J Community Hosp Intern Med Perspect, 2021
Bernard Soulier Syndrome is a genetically inherited platelet disorder that commonly presents with symptoms of impaired blood coagulation, such as epistaxis, menorrhagia, and petechiae formation. Here we present a case of Bernard Soulier Syndrome in which
Khan OA, Raashid S, Asghar S, Majeed R, Sherazi MF, Nayyer F, Anis A, Ehsan Z.   +7 more
europepmc   +2 more sources

Multivessel Percutaneous Coronary Intervention in a Patient With Bernard-Soulier Syndrome. [PDF]

JACC Case Rep, 2020
Bernard-Soulier syndrome, a congenital bleeding disorder, can rarely present with atherosclerosis and thrombosis. Acute coronary syndrome in such patients present a unique challenge as no standard set of guidelines exist for successful treatment.
Faheem O, Hussain B, Khurshid M, Hamid A, Rashid A.   +4 more
europepmc   +2 more sources

Bernard-Soulier syndrome (BSS) with uncontrollable menorrhagia. [PDF]

Asian J Transfus Sci, 2020
Menorrhagia is a common problem in women of reproductive age group and 5% of women between 30 and 49 years of age group consult their general practitioner for this problem.
Bhadra D, Chakraborty S.
europepmc   +2 more sources

Coexistence of Immune Thrombocytopenic Purpura and Bernard-Soulier Syndrome: A Rare Pediatric Case Report. [PDF]

Int Med Case Rep J
Sondus Alsharidah, Eman Almatar, Rania Lutfi, Omnia A Hashem Department of Hematology, NBK Specialized Children’s Hospital, Sabah, KuwaitCorrespondence: Eman Almatar, Department of Hematology, NBK Specialized Children’s Hospital, Sabah, Kuwait, Tel +965 ...
Alsharidah S, Almatar E, Lutfi R, Hashem OA.   +3 more
europepmc   +2 more sources

Anesthesia Management Using Remimazolam in A Patient With Bernard-Soulier Syndrome: A Case Report. [PDF]

Clin Case Rep
Bernard‐Soulier syndrome (BSS) is a platelet dysfunction disorder characterized by massive thrombocytopenia and a lack of platelet aggregation. Remimazolam, a short‐acting benzodiazepine sedative, is believed to have minimal effects on platelets.
Shakuo T, Ishida Y, Sugawara D, Ryo M, Okazaki H, Oe K.   +5 more
europepmc   +2 more sources

Novel Compound Heterozygous Mutations in Two Families With Bernard-Soulier Syndrome. [PDF]

Front Pediatr, 2020
Background: Bernard–Soulier Syndrome (BSS) is a rare autosomal recessive bleeding disorder with large platelets and thrombocytopenia. It is caused by homozygous or compound heterozygous mutations in the GP1BA, GP1BB, or GP9 genes, which together encode ...
Minkov M, Zeitlhofer P, Zoubek A, Kager L, Panzer S, Haas OA.   +5 more
europepmc   +2 more sources

Successful Vaginal Delivery in a Pregnant Woman With Bernard-Soulier Syndrome: A Case Report. [PDF]

Clin Case Rep
Bernard–Soulier syndrome (BSS) is a rare inherited platelet disorder that poses major risks during pregnancy because of potential bleeding complications. Managing such cases in low‐resource settings is especially challenging.
Yaghoubi M, Sabeti N, Hajmollarezaei E.
europepmc   +2 more sources

Bernard-Soulier syndrome or idiopathic thrombocytopenic purpura: A case series. [PDF]

Caspian J Intern Med, 2020
Background: Bernard-Soulier syndrome (BSS) is a rare, autosomal recessive platelet function disorder which is commonly mistaken for idiopathic thrombocytopenic purpura (ITP).The report includes seven cases of BSS that have been diagnosed and treated as ...
Reisi N.
europepmc   +2 more sources

Bernard-Soulier Syndrome: Identification of a Novel GP1BB Variant in a Mauritanian Patient. [PDF]

Mol Genet Genomic Med
Background Bernard‐Soulier syndrome (BSS) is a rare bleeding disorder caused by defects in the GPIb‐IX‐V complex, which is essential for platelet adhesion.
Salem ML, Zein E, Mohamed GS.
europepmc   +2 more sources