DIAGNOSING A CASE OF REKLINGAUZEN’S ILLNESS
Journal Title: World Science - Year 2018, Vol 3, Issue 5
Abstract
Reklingauzen’s illness is a widely spread genetic problem of humankind and it is a disease of genetic character. The reason is a mutation in one of the genes of chromosome 17. The peculiarity of Reklingauzen’s illness is that the appeared mutation has a high degree of clinical manifestation and transmitted by autosomal-dominant type.
Authors and Affiliations
V. R. Aitkulova, B. E. Kenenbayeva, N. R. Bender, D. U. Kaukenova, Y. G. Kot
Keywords
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