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Autor:
S. I. Bevz, N.M. Drobova, O.V. Piontkovska, K.O. Yanovska, V.A. Klymenko, O.V. Pasichnyk, N.T. Sindeeva
Publikováno v:
Sovremennaâ Pediatriâ, Iss 5(85), Pp 132-136 (2017)
The clinical case of the child with cystic fibrosis and severe delF508 CFTR mutation is described in the article. This patient died from multiorgan failure syndrome at 17 years old.