EARLY DIAGNOSIS AND TREATMENT IN PATIENT WITH A PRIMARY CILIARY DYSKINESIA (KARTAGENER SYNDROME): CASE REPORT

Primary ciliar dyskinesia is а rare orphan disease known for its multiple and variable symptoms caused by the marked genetic heterogenity beyond. As per the abundant symptoms in pediatric patients, a frequent inflammatory diseases of both upper and lower respiratory tract segments are the key points...

Full description

Bibliographic Details

Published in:	Архивъ внутренней медицины
Main Authors:	I. V. Rybakova, I. V. Koroleva, A. V. Khizhniak, O. V. Sidorovich, S. Iu. Elizarova
Format:	Article
Language:	Russian
Published:	SINAPS LLC 2018-08-01
Subjects:	primary ciliary dyskinesia kartagener syndrome
Online Access:	https://www.medarhive.ru/jour/article/view/813