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Titlebook: Inborn Metabolic Diseases; Diagnosis and Treatm John Fernandes,Jean-Marie Saudubray,N. R. M. Buist Book 19952nd edition Springer-Verlag Ber

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發(fā)表于 2025-3-21 18:19:18 | 只看該作者 |倒序?yàn)g覽 |閱讀模式
書(shū)目名稱(chēng)Inborn Metabolic Diseases
副標(biāo)題Diagnosis and Treatm
編輯John Fernandes,Jean-Marie Saudubray,N. R. M. Buist
視頻videohttp://file.papertrans.cn/464/463196/463196.mp4
圖書(shū)封面Titlebook: Inborn Metabolic Diseases; Diagnosis and Treatm John Fernandes,Jean-Marie Saudubray,N. R. M. Buist Book 19952nd edition Springer-Verlag Ber
描述Five years after its predecessor, the second edition of Inborn Metabolic Diseases: Diagnosis and Treatment is appearing in an almost completely revised form. Its main feature is an even stronger emphasis on the clinical presentation of inborn errors of metabolism. For that reason, clinical approach has not only remained the central theme of the first chapter, but also become the starting point for all chapters dealing with either a single specific disorder or a group of diseases. Particular attention has been paid to clinical presentation under acute, subacute or chronic forms, to the appearance of initially aspecific symptoms evolving into a more characteristic syn- drome at a later age, or vice versa, to clinical heterogeneity and its relation to genetic and biochemical heterogeneity. Brief reference to other diagnostic possibilities is also given in all disease-related chapters. Description of the metabolic derangements is restricted to the main pathophysiological features which provide the rationale for diagnosis and treatment. Methods to ascertain the diagnosis and diagnostic tests are listed comprehensively. As in the first edition, treatment is discussed extensively. Details
出版日期Book 19952nd edition
關(guān)鍵詞Aminos?uren; Kohlenhydrate; Lipidstoffwechsel; Neurotransmitter; Stoffwechselst?rungen; diagnosis; inborn
版次2
doihttps://doi.org/10.1007/978-3-662-03147-6
isbn_ebook978-3-662-03147-6
copyrightSpringer-Verlag Berlin Heidelberg 1995
The information of publication is updating

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Disorders of Galactose Metabolismy. Thus, galactose consumption is highest in infancy, and in those who are galactose intolerant toxic effects occur early in life. Therefore, detection after birth, rapid diagnosis, and immediate therapy are mandatory.
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TyrosineThree well-defined inborn errors of tyrosine catabolism are known:
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Urea Cycle DisordersFive inherited disorders of the . are now well described. These are characterised by . and disordered amino acid metabolism. The presentation is highly variable: those presenting in the newborn period usually have an overwhelming illness, but the presentation may be subtle in those who present later in childhood or adult life.
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Disorders of Fructose Metabolismisphosphatase deficiency, sometimes also considered an inborn error of fructose metabolism, will be discussed in Chap. 8. It is manifested by the appearance of hypoglycemia and lactic acidosis during fasting and may also be life-threatening.
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