Catheter Intervention in a Patient with Intracranial Aneurysms and Glanzmann Thrombasthenia Caused by a Novel Homozygous Likely Pathogenic Variant in the

Glanzmann Thrombasthenia (GT) ITGA2B gene catheter intervention inherited platelet disorder

Journal

Diseases (Basel, Switzerland)
ISSN: 2079-9721
Titre abrégé: Diseases
Pays: Switzerland
ID NLM: 101636232

Informations de publication

Date de publication:
27 Jun 2024
Historique:
received: 14 05 2024
revised: 19 06 2024
accepted: 19 06 2024
medline: 26 7 2024
pubmed: 26 7 2024
entrez: 26 7 2024
Statut: epublish

Résumé

Glanzmann Thrombasthenia (GT) is an inherited platelet disorder caused by defects in platelet integrin α

Identifiants

pubmed: 39057107
pii: diseases12070136
doi: 10.3390/diseases12070136
pii:
doi:

Types de publication

Case Reports Journal Article

Langues

eng

Subventions

Organisme : CSL Behring
ID : ZVS-2019092402

Auteurs

Doris Boeckelmann (D)

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center-University of Freiburg, 79106 Freiburg, Germany.

Lara von Dobeneck (L)

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center-University of Freiburg, 79106 Freiburg, Germany.

Hans Henkes (H)

Neuroradiological Clinic, Klinikum Stuttgart, 70174 Stuttgart, Germany.
Institute for Diagnostic and Interventional Radiology and Neuroradiology, University Hospital Essen, 45147 Essen, Germany.

Hermann Eichler (H)

Institute of Clinical Hemostaseology and Transfusion Medicine, Saarland University and University Hospital, 66424 Homburg, Germany.

Hannah Glonnegger (H)

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center-University of Freiburg, 79106 Freiburg, Germany.

Barbara Zieger (B)

Department of Pediatrics and Adolescent Medicine, Division of Pediatric Hematology and Oncology, Medical Center-University of Freiburg, 79106 Freiburg, Germany.

Classifications MeSH