jour
 2022
DOI: 10.18705/2782-3806-2022-2-2-129-136
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Combination of two rare genetically determinated diseases, associated with poor prognosis, in a 2-year-old child

Е. S. Sivushchina
1
,
A. S. Myravyev
2
,
T. S. Kovalchuk
3
et al.

Abstract: This article presents the case of a combination of two genetically determined diseases in one early age patient: long QT syndrome type 1 and mucopolysaccharidosis type IIIA.

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