TY  - JOUR
T1  - Cystic fibrosis diagnosed in a nineteen-year-old case
AU  - Yılmaz, Meltem
AU  - Mutlu, Levent
PY  - 2023
DA  - November
Y2  - 2023
DO  - 10.18621/eurj.1207253
JF  - The European Research Journal
JO  - Eur Res J
PB  - Prusa Medical Publishing
WT  - DergiPark
SN  - 2149-3189
SP  - 1537
EP  - 1540
VL  - 9
IS  - 6
LA  - en
AB  - Cystic fibrosis is the most common autosomal recessive hereditary disease in white populations. It is characterized by the formation of abnormal secretions in the exocrine glands located in the sweat and salivary glands, tracheobronchial tree, large intestine, and pancreas. The severity of the clinic depends on the type of "cystic fibrosis transmembrane regulatory protein" gene mutation. Although most cases are diagnosed in infancy or childhood, some patients are also diagnosed during adolescence and adulthood. We report a case of a 19-year-old patient who was followed up with a diagnosis of asthma and bronchiectasis since childhood and diagnosed with cystic fibrosis.
KW  - Adolescence
KW  - bronchiectasis
KW  - cystic fibrosis
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UR  - https://doi.org/10.18621/eurj.1207253
L1  - https://dergipark.org.tr/en/download/article-file/2782863
ER  -