GALACTOSEMIA MKB 10: E74

Authors

  • Hamrayev Javohir Student of the 108th group of the Faculty of Pediatrics of the Samarkand State Medical University Author

Keywords:

alactosemia, MKB 10, enzyme, chromosome, amino acid, autosomal chromosome, mutation, recessive, toxic poisoning, lactose, galactose, glucose, galactose-1 phosphaturidyltransferase, cataract, amniotic fluid, GALK, GALK1, osteoporosis, Diet, Mendelian inheritance, Liver cirrhosis, jaundice, hypotension, lethargy, hypogonadism, diarrhea, homozygous, heterozygous.

Abstract

In this article, we will consider galactosemia, a disease associated with impaired enzyme activity. Who identified galaztosemia. Let's look at the origin of the disease, its symptoms, heredity, prevention and diagnosis. It talks about the methods of treatment of the disease and prevention of the disease.

References

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Published

2024-03-27