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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| Główni autorzy: | , , , , |
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| Format: | Artigo |
| Język: | Russo |
| Wydane: |
SINAPS LLC
2018-08-01
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| Seria: | Архивъ внутренней медицины |
| Hasła przedmiotowe: | |
| Dostęp online: | https://www.medarhive.ru/jour/article/view/813 |
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