Nutrition Management of Inherited Metabolic Diseases Lessons from Metabolic University
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Editura: Springer
Limba: Engleza
Nr. pagini: 392
Coperta: Paperback
Dimensiuni: 17.8 x 2.4 x 25.4 cm
An aparitie: 2015
- Offers guidance on current nutrition treatment of a wide range of inherited metabolic diseases
- Draws on 7 years of lectures delivered through Metabolic University
- Designed to ensure ease of reference for clinicians
About this book
This up-to-date reference on the nutrition management of inherited metabolic diseases (IMD) covers a wide range of these disorders, including phenylketonuria and other aminoacidopathies, organic acidemias, urea cycle disorders, fatty acid oxidation disorders, galactosemia and glycogen storage diseases. Guidance is also provided on laboratory evaluations and biochemical testing and monitoring.
Topics such as newborn screening for IMD, as well as nutrition management during pregnancy and transplantation, are addressed. The book is based on 7 years of lectures delivered through Metabolic University an interactive, didactic program designed to provide training to dietitians who work with individuals with IMD. This book provides the basic information required to manage nutrition care and is a resource for clinicians new to this complex field.
Table of contents (27 chapters)
· Introduction to Genetics
Freehauf, Cynthia
Pages 3-14
· Expanded Newborn Screening for Inherited Metabolic Diseases
Wright, Erica L.
Pages 15-23
· Nutrition Education
Bernstein, Laurie E. (et al.)
Pages 25-33
· Pathophysiology of Inherited Metabolic Disease
Baker, Peter R.
Pages 35-45
· Metabolic Intoxication Syndrome in a Newborn
Giżewska, Maria
Pages 47-57
· Anabolism: Practical Strategies
Hove, Johan L. K.
Pages 59-62
· Protein Requirements in Inherited Metabolic Diseases
Yannicelli, Steven
Pages 63-73
· Laboratory Evaluations in Inherited Metabolic Diseases
Coughlin, Curtis R.
Pages 75-85
· Phenylketonuria: Phenylalanine Neurotoxicity
Giżewska, Maria
Pages 89-99
· Phenylketonuria: The Diet Basics
Calcar, Sandy
Pages 101-116
· Understanding Large Neutral Amino Acids and the Blood-Brain Barrier
Yannicelli, Steven
Pages 117-125
· Tetrahydrobiopterin Therapy for Phenylketonuria
Jurecki, Elaina
Pages 127-138
· Maternal Phenylketonuria
Rohr, Fran
Pages 139-147
· Homocystinuria: Diagnosis and Management
Thomas, Janet A.
Pages 149-158
· Nutrition Management of Urea Cycle Disorders
Rohr, Fran
Pages 159-171
· Nutrition Management of Maple Syrup Urine Disease
Calcar, Sandy
Pages 173-183
· Organic Acidemias
Thomas, Janet A.
Pages 187-201
· Glutaric Acidemia Type I: Diagnosis and Management
Coughlin, Curtis R.
Pages 203-209
· Nutrition Management of Glutaric Acidemia Type 1
Bernstein, Laurie E.
Pages 211-220
· Nutrition Management of Propionic Acidemia and Methylmalonic Acidemia
Calcar, Sandy
Pages 221-228
· Nutrition Management During Pregnancy: Maple Syrup Urine Disease, Propionic Acidemia, Methylmalonic Acidemia, and Urea Cycle Disorders
Calcar, Sandy
Pages 229-237
· Fatty Acid Oxidation Defects
Hove, Johan L. K.
Pages 241-254
· Nutrition Studies in Long-Chain Fatty Acid Oxidation Disorders: Diet Composition and Monitoring
Gillingham, Melanie Boyd
Pages 255-270
· Nutrition Management of Fatty Acid Oxidation Disorders
Rohr, Fran
Pages 271-282
· The Diet for Galactosemia
Bernstein, Laurie E. (et al.)
Pages 285-293
· Glycogen Storage Diseases
Hove, Johan L. K.
Pages 295-305
· Nutrition Management of Glycogen Storage Disease Type 1
Calcar, Sandy
Pages 307-317
ebookshop
An aparitie | 2015 |
Autor | Bernstein, Laurie E., Rohr, Fran, Helm, Joanna R (Eds.) |
Dimensiuni | 17.8 x 2.4 x 25.4 cm |
Editura | Springer |
Format | Paperback |
ISBN | 9783319146201 |
Limba | Engleza |
Nr pag | 392 |
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