Wildhaber J, Seelentag W K, Spiegel R, Schöni M H
University Children's Hospital, Zurich, Switzerland.
J Pediatr Surg. 1996 Jul;31(7):951-4. doi: 10.1016/s0022-3468(96)90419-4.
The authors present the case of a newborn girl who had cystic fibrosis associated with neuronal intestinal dysplasia type B (NID-B). The association is rare but must be considered in the differential diagnosis of gastrointestinal problems in patients with cystic fibrosis. The present case elucidates the intestinal problems that can arise with this combination of diseases. Although the unusual association found in this patient could have been a random occurrence, the possibility of an NID-B determining gene localized on chromosome 7q should be considered.
作者报告了一例患有囊性纤维化并伴有B型神经元性肠发育异常（NID - B）的新生女婴病例。这种关联很罕见，但在囊性纤维化患者胃肠道问题的鉴别诊断中必须予以考虑。本病例阐明了这种疾病组合可能出现的肠道问题。尽管在该患者中发现的这种不寻常关联可能是偶然发生的，但应考虑位于7号染色体长臂上的NID - B决定基因的可能性。
