Genetic Metabolism Disorders in Newborn

  • Owayes Muaffaq Hamed Department of Biology, Faculty of Science, University of Mosul, IRAQ
  • Amjad Abdul-hadi Mohammed Department of Biology, Faculty of Science, University of Mosul, IRAQ
  • Raed Salem Alsaffar Department of Biology, Faculty of Science, University of Mosul, IRAQ
Keywords: Genetic Disease, Newborn, Metabolism Disorders

Abstract

Babies with any type of metabolic disorders lack the ability to break down the food well, which may induce too little amino acids, phenylalanine and blood sugar to the body, there are numerous kinds of this disorders, most of babies with a genetic metabolic disease have many mutation in gene that coded an enzyme which results a deficiency in same enzyme are hundreds of these disorders and they were diagnosed by their symptoms and the treatment method. The treatment methods of the metabolic disorder depend on the specific type of disorders, inborn metabolic disease are some-time  treated with dietary guidance, and other childcare choices, many hereditary metabolic disease are initially caused by gene mutations and that transferred from parents to offspring.

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Published
2021-01-13
How to Cite
Owayes Muaffaq Hamed, Amjad Abdul-hadi Mohammed, & Raed Salem Alsaffar. (2021). Genetic Metabolism Disorders in Newborn. International Journal for Research in Applied Sciences and Biotechnology, 8(1), 77-81. https://doi.org/10.31033/ijrasb.8.1.9