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Inherited Disease Epidemiology Study as the Source for Pharmacotherapy Need Determination among infants
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| Author:
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INNA SOROKINA, SVETLANA V. VINOGLYADOVA, NATALIA A. RUDYH, IRINA N. BEZMENOVA, IRINA N. VERZILINA, VALENTINA S. ORLOVA
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| Abstract:
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Based on the data gate by taking newborns in the Belgorod region (2006 - 2013) this study defined the frequencies of genetic metabolic diseases to discover the necessity for pharmacotherapy. The frequency of phenylketonuria (PKU) among newborns made 1:7831, cystic fibrosis (MV) - 1: 12103, congenital hypothyroidism (CH) - 1:4930, adrenogenital syndrome (AGS) - 1:13313, galactosemia (GAL) - 1:33284. There are 58 children with hereditary metabolic diseases and the need of pharmacotherapy in the Belgorod region (2006 - 2013).
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| Keyword:
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hereditary diseases, metabolism, screening, phenylketonuria, cystic fibrosis, congenital hypothyroidism
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| EOI:
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-
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| DOI:
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https://doi.org/10.31838/ijpr/2019.11.04.0316
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| Download:
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Request For Article
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