OBJECTIVE:
If situs inversus is seen on chest x-ray and the patient's clinic is compatible with primary ciliary dyskinesia (PSD), it should be examined in more detail and screened for siblings in case of PSD. In addition, we aimed to state that even if the directional markers are not used correctly on the chest radiography, even an obvious condition such as situs inversus may be omitted or radiographs may be misinterpreted by the physician.
CASE:
Twelve years old girl with primary ciliary dyskinesia was evaluated. The presence of recurrent sinopulmonary infection and laterality defect on chest x-ray led to the investigation of PSD and the diagnosis of PSD was confirmed by homozygous variant in CCDC39 gene.
CONCLUSION:
The literature review shows that some of the radiographs have incorrect or no anatomical direction markers. In our case, if the radiography contains an incomplete directional marker, it may lead to delayed diagnosis and wrong treatment for the patient. Screening of siblings for a genetic disease such as PSD will provide many benefits.
Ciliary Motility Disorders Genetic Diseases Congenital Abnormalities
Birincil Dil | İngilizce |
---|---|
Konular | Sağlık Kurumları Yönetimi |
Bölüm | Konferans Bildirisi (Tam Metin) |
Yazarlar | |
Yayımlanma Tarihi | 10 Aralık 2019 |
Kabul Tarihi | 16 Ocak 2020 |
Yayımlandığı Sayı | Yıl 2019 Cilt: 7 Sayı: Ek - IRUPEC 2019 Kongresi Tam Metin Bildirileri |