Artikel: Analysis of Clinical Manifestations, Imaging Features, and Gene Mutation Characteristics of 6 Children with Cystic Fibrosis in China.
Evidence-based complementary and alternative medicine : eCAM
2021 Band 2021, Seite(n) 7254391
Abstract: Objective: To explore the clinical manifestations, imaging features, and gene mutation characteristics of 6 children with cystic fibrosis (CF) so as to improve the understanding and diagnosis awareness of CF in children and reduce the missed diagnosis ... ...
Abstract | Objective: To explore the clinical manifestations, imaging features, and gene mutation characteristics of 6 children with cystic fibrosis (CF) so as to improve the understanding and diagnosis awareness of CF in children and reduce the missed diagnosis and misdiagnosis. Methods: The clinical manifestations, imaging, and gene mutation data of six children with CF were collected and retrospectively analyzed. Results: Among the 6 cases of CF, there were 4 males and 2 females. Among the 6 children with CF, 5 cases presented with recurrent respiratory tract infection. Etiology suggested 3 cases of Conclusion: CF is a disease caused by CFTR mutation. The incidence of this disease in China is low, and the clinical manifestations have great differences. The main symptoms are respiratory symptoms. Some children have gastrointestinal symptoms and/or PBS, and some children only show a single systemic lesion. |
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Sprache | Englisch |
Erscheinungsdatum | 2021-11-02 |
Erscheinungsland | United States |
Dokumenttyp | Journal Article ; Retracted Publication |
ZDB-ID | 2171158-6 |
ISSN | 1741-4288 ; 1741-427X |
ISSN (online) | 1741-4288 |
ISSN | 1741-427X |
DOI | 10.1155/2021/7254391 |
Datenquelle | MEDical Literature Analysis and Retrieval System OnLINE |
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