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Titlebook: Studies in Inherited Metabolic Disease; Prenatal and Perinat G. M. Addison,J. M. Connor,R. J. Pollitt Book 1989 SSIEM and Kluwer Academic P

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书目名称Studies in Inherited Metabolic Disease
副标题Prenatal and Perinat
编辑G. M. Addison,J. M. Connor,R. J. Pollitt
视频video
图书封面Titlebook: Studies in Inherited Metabolic Disease; Prenatal and Perinat G. M. Addison,J. M. Connor,R. J. Pollitt Book 1989 SSIEM and Kluwer Academic P
描述With improved control of most environmental causes of disease, genetic illness has assumed a primary importance in the causation of handicap and mortality in all age groups. At present, effective therapy is available for relatively few genetic conditions and prenatal diagnosis is an important option for couples at high risk. The task of providing prenatal diagnosis for these couples requires a team approach between clinicians and scientists, and is complicated by the large number of diverse conditions and by the rapid developments in the field, both obstetric in relation to imaging and tissue sampling methods and genetic in relation to techniques for analysis. Against this background, the aim of the Symposium was to provide an overview of the current status of prenatal and perinatal diagnosis of inborn errors of metabolism. The format consisted of the usual mixture of specific invited overviews and free communications in either oral or poster form. The invited overviews, as can be seen from this publication, covered a wide range, from accepted methods for neonatal diagnosis and screening to newer techniques for prenatal diagnosis and likely future developments with respect to gene
出版日期Book 1989
关键词Galactose; Glycogen; enzymes; gene therapy; metabolism; transplantation
版次1
doihttps://doi.org/10.1007/978-94-009-1069-0
isbn_softcover978-94-010-6970-0
isbn_ebook978-94-009-1069-0
copyrightSSIEM and Kluwer Academic Publishers 1989
The information of publication is updating

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Prenatal Diagnosis of Disorders of Galactose Metabolismvillus biopsies and by galactitol estimation in amniotic fluid supernatant. Although the long-term outcome of patients treated on a galactose-restricted diet is recognized to be unsatisfactory, prenatal diagnosis is only rarely performed with a view to terminating the affected pregnancy.
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Prefacesampling methods and genetic in relation to techniques for analysis. Against this background, the aim of the Symposium was to provide an overview of the current status of prenatal and perinatal diagnosis of inborn errors of metabolism.
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The Salience of Garrod’s ‘Molecular Groupings’ and ‘Inborn Factors in Disease’nzymes are normally homopolymeric; (3) in clinical severity of ‘monogenic’ disease (e.g. familial hypercholesterolaemia and muscular dystrophy) when variation is not explained by allelic heterogeneity. The associated chemical individuality in each case can be used to identify risk and thus as a mode of predictive medicine.
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A Clinician’s View of the Mass Screening of the Newborn for Inherited Diseases: Current Practice and. A simple tool for early detection is now available and the population afflicted with a mutant gene which causes major health problems should receive special attention from its government. It is too early to offer any comment about cystic fibrosis screening; further developments must be awaited.
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A Clinical Biochemist’s View of the Investigation of Suspected Inherited Metabolic Diseasevidual patient. A full metabolic laboratory investigation programme is described and illustrated with some examples of abnormal metabolite patterns. Diagnostic results over a 2-year period are presented.
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