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...

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Bibliographic Details
Main Authors: I. V. Rybakova (Author), I. V. Koroleva (Author), A. V. Khizhniak (Author), O. V. Sidorovich (Author), S. Iu. Elizarova (Author)
Format: Book
Published: SINAPS LLC, 2018-08-01T00:00:00Z.
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3rd Floor Main Library

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Call Number: A1234.567
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