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Titlebook: Inborn Metabolic Diseases; Diagnosis and Treatm Jean-Marie Saudubray,Matthias R. Baumgartner,John Book 2022Latest edition Springer-Verlag

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書目名稱Inborn Metabolic Diseases
副標題Diagnosis and Treatm
編輯Jean-Marie Saudubray,Matthias R. Baumgartner,John
視頻videohttp://file.papertrans.cn/464/463195/463195.mp4
概述A clinical and biochemical approach to the diagnosis and management of IEM.Indispensable for professionals in pediatrics, neonatology, pathological biochemistry, genetics, neurology.Written by interna
圖書封面Titlebook: Inborn Metabolic Diseases; Diagnosis and Treatm Jean-Marie Saudubray,Matthias R. Baumgartner,John  Book 2022Latest edition Springer-Verlag
描述.This 7th edition is a milestone in the series of Inborn Metabolic Diseases (IMD), recognised as the standard textbook for professionals involved in the diagnosis and management of IMD..Within the last 5 years a Copernican revolution in our understanding of IMD has changed the definition, concepts, paradigms, and classification. This new edition now extends the concept of IMD to include those disturbances in molecular machinery diagnosed by molecular techniques but currently without measurable metabolic markers..The book presents a clinical and biochemical approach to the diagnosis and management of IEM with many diagnostic algorithms for patients of all ages and with a particular focus on neurological presentations. It includes separate, comprehensive sections on IEM classified in 3 major pathophysiological categories: disorders of energy metabolism, both mitochondrial and non-mitochondrial; small molecule disorders, mostly diagnosed with metabolic markers; and complex molecules disorders, mostly diagnosed with molecular techniques..Two new chapters were added, describing around 600 disorders of nucleic acid metabolism, tRNA metabolism, ribosomal biogenesis, and cellular trafficki
出版日期Book 2022Latest edition
關鍵詞Disorders of metabolism; Inborn errors of metabolism; Inherited metabolic diseases; Metabolic diseases;
版次7
doihttps://doi.org/10.1007/978-3-662-63123-2
isbn_softcover978-3-662-63125-6
isbn_ebook978-3-662-63123-2
copyrightSpringer-Verlag GmbH Germany, part of Springer Nature 2022
The information of publication is updating

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The Glycogen Storage Diseases and Related Disorderstic glycogenosis generally cause hepatomegaly (apart from GSD 0a) and fasting hypoglycaemia whereas the muscle disorders are associated with skeletal and/or cardiomyopathy. The clinical phenotypes are extremely heterogeneous.
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Congenital Hyperinsulinism and Genetic Disorders of Insulin Resistance and Signalling recurrent severe hypoglycaemia in neonates, in whom a delayed diagnosis or inappropriate medical management is responsible for brain damage in more than 30%, underlining the importance of an early diagnosis and of an urgent care.
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