Sonnappa Samatha, Prescott Katrina, Adler Beryl, Dinwiddie Robert, Wallis Colin
Department of Respiratory Medicine, Great Ormond Street Hospital, London, UK.
Pediatr Pulmonol. 2005 Aug;40(2):166-8. doi: 10.1002/ppul.20254.
A 6-year-old Asian girl was diagnosed with cystic fibrosis at 3 months of age, following investigations for failure to thrive. She had intrauterine growth retardation and continued to have restricted postnatal growth, despite adequate caloric intake and enzyme replacement therapy. Further investigations were initiated when she was 5 years old, as her growth was not responding to the usual treatment measures. These tests revealed that she had maternal isodisomy of chromosome 7.
一名6岁亚洲女孩在3个月大时因生长发育迟缓接受检查,被诊断出患有囊性纤维化。她有宫内生长迟缓,尽管摄入了足够的热量并接受了酶替代疗法,但出生后生长仍受限。5岁时,由于她的生长对常规治疗措施没有反应,因此展开了进一步检查。这些检查显示她存在7号染色体的母源同二体。