Amat L, Martín E, Matéu L, Rubio C, Ballesta A
An Esp Pediatr. 1978 Mar;11(3):219-26.
A case of Congenital deficiency of Enterokynase is presented. The main clinical findings are: Chronic diarrhea, malnutrition and edema. Diagnosis was made by determination of tripsine activity in duodenal juice before and later to confront it to Enterokynase. The patient was treated with pancreatic supplements and protein hidrolysate with favourable results.
本文报告一例先天性肠激酶缺乏症病例。主要临床症状为:慢性腹泻、营养不良和水肿。通过测定十二指肠液中胰蛋白酶活性,并与肠激酶进行对比来做出诊断。该患者接受了胰腺补充剂和蛋白水解物治疗,效果良好。