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PCR in the Analysis of Clinical Samples: Prenatal and Postnatal Diagnosis of Inborn Errors of Metabolism

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Orientador(es)

Resumo(s)

Inborn errors of metabolism (IEMs) are individually rare but collectively common. As more and more enes are cloned and specific disease-causing mutations are identified, the diagnosis of IEMs is becoming increasingly confirmed by mutation analysis. Diagnosis is important not only for treatment and prognosis but also for genetic counselling and prenatal diagnosis in subsequent pregnancies. A wide range of molecular methods is available for the identification of mutations and other DNA variants, most of which are based on the Polymerase Chain Reaction (PCR). In this chapter, we focus on PCR-based methods for the detection of point mutations or small deletions/insertions as these are the most frequent causes of IEMs.

Descrição

Palavras-chave

PCR IEM Prenatal Molecular Diagnosis Postnatal Molecular Diagnosis Doenças Genéticas

Contexto Educativo

Citação

Methods Mol Biol. 2017;1620:213-224. doi: 10.1007/978-1-4939-7060-5_15.

Projetos de investigação

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Fascículo

Editora

Springer Science and Business Media

Licença CC

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