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Acid Sphingomyelinase Deficiency

Om Acid Sphingomyelinase Deficiency

Acid Sphingomyelinase Deficiency is a rare genetic disorder that affects many parts of the body, including the liver, spleen, lungs, and brain. This book provides a comprehensive overview of the disease, including its causes, symptoms, and management. It covers a wide range of topics, from the medical aspects of the disease to financial planning and career guidance for patients and their families. The book also highlights the latest research on Acid Sphingomyelinase Deficiency and the challenges and opportunities that lie ahead in improving the lives of those affected by the disease. This book is an essential resource for patients, families, healthcare professionals, and researchers seeking a deeper understanding of Acid Sphingomyelinase Deficiency. With its accessible language, this book will serve as a valuable guide and source of inspiration for anyone impacted by this rare disease.

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  • Språk:
  • Engelsk
  • ISBN:
  • 9789357333382
  • Bindende:
  • Paperback
  • Sider:
  • 172
  • Utgitt:
  • 6 juni 2023
  • Dimensjoner:
  • 152x10x229 mm.
  • Vekt:
  • 259 g.
  Gratis frakt
Leveringstid: 2-4 uker
Forventet levering: 22 oktober 2024

Beskrivelse av Acid Sphingomyelinase Deficiency

Acid Sphingomyelinase Deficiency is a rare genetic disorder that affects many parts of the body, including the liver, spleen, lungs, and brain. This book provides a comprehensive overview of the disease, including its causes, symptoms, and management. It covers a wide range of topics, from the medical aspects of the disease to financial planning and career guidance for patients and their families. The book also highlights the latest research on Acid Sphingomyelinase Deficiency and the challenges and opportunities that lie ahead in improving the lives of those affected by the disease. This book is an essential resource for patients, families, healthcare professionals, and researchers seeking a deeper understanding of Acid Sphingomyelinase Deficiency. With its accessible language, this book will serve as a valuable guide and source of inspiration for anyone impacted by this rare disease.

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