Abstract
CF is considered a rare disease among the non-Caucasian population. The
clinical phenotypes and genotypic spectrum of Chinese CF patients are
reported to be different from that observed in
Caucasians[(1)](#ref-0001). Our patient carried compound
heterozygous mutations which are not included in the Caucasian CFTR
common mutation-screening panel and have not been reported yet. CFTR
dysfunction causes a spectrum of diseases, with a range in the number of
organs involved and varying disease severity. Typical phenotypic
features of CF include respiratory diseases (bronchiectasis with
persistent airway-based infection and inflammation), gastrointestinal
diseases (meconium ileus (MI)), hepatobiliary manifestations (pancreatic
insufficiency), and male infertility[(2)](#ref-0002). Our patient
presented severe manifestations, namely colonic perforation, meconium
thorax, severe pneumonia, diaphragmatic defects-caused marked diaphragm
elevation and respiratory failure. It’s difficult to ascertain whether
the diaphragmatic defects in our patient is related to CF. MI is often
the first manifestation of CF and occurs in approximately 20% of CF
patients. CF should therefore be high in the differential diagnosis of
any infant presenting with MI[(3)](#ref-0003).