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1.
Journal of the Korean Pediatric Society ; : 1083-1091, 1981.
Article in Korean | WPRIM | ID: wpr-10320

ABSTRACT

No abstract available.


Subject(s)
IgA Vasculitis
2.
Journal of the Korean Pediatric Society ; : 1003-1008, 1979.
Article in Korean | WPRIM | ID: wpr-41007

ABSTRACT

The authors experienced a case of generalized bytomegalic inclusion diseas, characterized by numerous petechiae associated with anemia and hepatomegly, in the premature infant who was hypotonic and cyanosed, with respiratory difficulty and an Apgar score of 4 at 1 minute. The rapid deterioration of the case condition was followed by the death occurring nine hours after birth. The diagnosis was confirmed by the autopsy, and a brief review of the literature was made.


Subject(s)
Humans , Infant, Newborn , Anemia , Apgar Score , Autopsy , Cytomegalovirus Infections , Diagnosis , Infant, Premature , Parturition , Purpura
3.
Journal of the Korean Pediatric Society ; : 1159-1162, 1978.
Article in Korean | WPRIM | ID: wpr-189445

ABSTRACT

One of the rarest anomalies of the urinary tract is crossed renal ectopia. In Crossed Renal Ectopia, the kidney may be fused or unfused. The fused type is more common. The Diagnosis is made by a combination of urologic and radiologic technics including intravenous pyelography, Cytoscopic examination, retrograde pyelography and retroperitoneal air insufflation. The treatment of renal ectopia without fusion is that of the complicating disease in a kindney normally placed. This paper presented one care of crossed renal ectopia with fusion in a 5 month old female patient who admitted with high fever, oliguria and a palpable abdominal mass. The literatures were reviewed briefly.


Subject(s)
Female , Humans , Infant , Diagnosis , Fever , Insufflation , Kidney , Oliguria , Urinary Tract , Urography
4.
Journal of the Korean Pediatric Society ; : 988-991, 1977.
Article in Korean | WPRIM | ID: wpr-11739

ABSTRACT

A case of congenital diaphragmatic hernia in a newborn was presented, who had characteristic clinical and X-ray findings. The case manifested dyspnea, cyanosis and shift of the heart and mediastinum to the right immediately after birth, which was throught to be congenital diaphragmatic hernia and verified by autopsy. On autopsy, a large left diaphragmatic defect resulting massive diaphragmatic hernia and ipsilateral pulmonary hypoplasia were found. The authors report the case with review of pertinent literature.


Subject(s)
Humans , Infant, Newborn , Autopsy , Cyanosis , Dyspnea , Heart , Hernia, Diaphragmatic , Lung , Mediastinum , Parturition
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