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

RESUMEN

No abstract available.


Asunto(s)
Vasculitis por IgA
2.
Journal of the Korean Pediatric Society ; : 1003-1008, 1979.
Artículo en Coreano | WPRIM | ID: wpr-41007

RESUMEN

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.


Asunto(s)
Humanos , Recién Nacido , Anemia , Puntaje de Apgar , Autopsia , Infecciones por Citomegalovirus , Diagnóstico , Recien Nacido Prematuro , Parto , Púrpura
3.
Journal of the Korean Pediatric Society ; : 1159-1162, 1978.
Artículo en Coreano | WPRIM | ID: wpr-189445

RESUMEN

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.


Asunto(s)
Femenino , Humanos , Lactante , Diagnóstico , Fiebre , Insuflación , Riñón , Oliguria , Sistema Urinario , Urografía
4.
Journal of the Korean Pediatric Society ; : 988-991, 1977.
Artículo en Coreano | WPRIM | ID: wpr-11739

RESUMEN

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.


Asunto(s)
Humanos , Recién Nacido , Autopsia , Cianosis , Disnea , Corazón , Hernia Diafragmática , Pulmón , Mediastino , Parto
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