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...
Saved in:
| Main Authors: | , , , , |
|---|---|
| 格式: | Article |
| 語言: | 俄语 |
| 出版: |
SINAPS LLC
2018-08-01
|
| 叢編: | Архивъ внутренней медицины |
| 主題: | |
| 在線閱讀: | https://www.medarhive.ru/jour/article/view/813 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|