Fast Facts: Pyruvate Kinase Deficiency

Bertil Glader

ISBN 10: 3318072559 / ISBN 13: 9783318072556

Edité par Karger Verlag Apr 2025, 2025

A propos de cet article

Neuware -Pyruvate kinase (PK) deficiency is an inherited disease that affects red blood cells and manifests as hemolytic anemia. It is a lifelong condition, with symptoms that range from mild to severe. Despite an ever-growing understanding of its pathophysiology, etiology, and epidemiology, and an active research program, PK deficiency remains unfamiliar to many medical practitioners. PK deficiency is clinically heterogeneous, so healthcare professionals need to consider the possibility of this disorder in all patients with a congenital hemolytic anemia.

N° de réf. du vendeur 9783318072556

Détails bibliographiques

• Titre: Fast Facts: Pyruvate Kinase Deficiency
• Éditeur: Karger Verlag Apr 2025
• Date de parution: 2025
• Langue: anglais
• ISBN à 10 chiffres: 3318072559
• ISBN à 13 chiffres: 9783318072556
• Reliure: Taschenbuch
• État de l'article: Neu

A propos de ce titre

Synopsis

Pyruvate kinase (PK) deficiency is an inherited disease that affects red blood cells and manifests as hemolytic anemia. It is a lifelong condition, with symptoms that range from mild to severe. Despite an ever-growing understanding of its pathophysiology, etiology, and epidemiology, and an active research program, PK deficiency remains unfamiliar to many medical practitioners. PK deficiency is clinically heterogeneous, so healthcare professionals need to consider the possibility of this disorder in all patients with a congenital hemolytic anemia.