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Medico-Social Management of Inherited Metabolic Disease
Engelsk Paperback
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kr 99
Medico-Social Management of Inherited Metabolic Disease
Engelsk Paperback
The study of inherited metabolic disease became a subject of more than academic interest in 1953 when Bickel, Gerrard and Hickmans dis­ covered that the totally disabling consequences of phenylketonuria could be prevented if treatment was instituted in the first months of life. This required the widespread screening of all newborn babies and 7 years later this had been successfully achieved in the United King­ dom. The next 10 years was a period of consolidation: screening methods were improved and extended to include other disorders; treatment of phenylketonuria was vastly improved with the stimulus of the increasing numbers of patients being detected, and research into new forms of therapy for some of the other disorders being detected has been initiated. The success of this scheme is illustrated by the remarkable achievement reported by the Phenylketonuria Registry referred to in the present volume. But at what cost has this progress been made? It is unnecessary to discuss the financial cost for many of the developments would not have been started if their economic value in the system of health care had not been unequivocally established.
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The study of inherited metabolic disease became a subject of more than academic interest in 1953 when Bickel, Gerrard and Hickmans dis­ covered that the totally disabling consequences of phenylketonuria could be prevented if treatment was instituted in the first months of life. This required the widespread screening of all newborn babies and 7 years later this had been successfully achieved in the United King­ dom. The next 10 years was a period of consolidation: screening methods were improved and extended to include other disorders; treatment of phenylketonuria was vastly improved with the stimulus of the increasing numbers of patients being detected, and research into new forms of therapy for some of the other disorders being detected has been initiated. The success of this scheme is illustrated by the remarkable achievement reported by the Phenylketonuria Registry referred to in the present volume. But at what cost has this progress been made? It is unnecessary to discuss the financial cost for many of the developments would not have been started if their economic value in the system of health care had not been unequivocally established.
Produktdetaljer
Sprog: Engelsk
Sider: 310
ISBN-13: 9789401161756
Indbinding: Paperback
Udgave:
ISBN-10: 9401161755
Kategori: Pædiatri
Udg. Dato: 12 mar 2012
Længde: 0mm
Bredde: 235mm
Højde: 155mm
Oplagsdato: 12 mar 2012
Forfatter(e):
Forfatter(e)


Kategori Pædiatri


Sprog Engelsk


Indbinding Paperback


Sider 310


Udgave


Længde 0mm


Bredde 235mm


Højde 155mm


Udg. Dato 12 mar 2012


Oplagsdato 12 mar 2012

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