|
Statistical analysis of outpatients and inpatients from 1985 to 1988 was assessed with aims to have an overal grasp of patterns and trends of childhood diseases at Seoul National University Children, s Hospital. 1) Number of outpatient visits were totally 458,390 with annual number of visits of 144,754 and average daily number of 461, including 241 visits in Department of Pediatrics. 2) Number of patients at Eemergency... |
Modem medical science has been developed advanced rapidly in the past years, but congenital anomalies are known as a major cause of neonatal death. So, we studied the incidence of congenital malformations among 11,119 babies deliveried or admitted at EWUH during a period of five years starting from June 1983. The results were as follows: 1) The incidence of congenital malformations among 11,119 deliveries was 1.5%(1.5%... |
The C-reactive protein is an abnormal protein, which is reacted to various non-specific stmuli such as infection, tissue necrosis, trauma, neoplasm and granuloma formation. Hence, C-reactive protein was index of infection and its allied diseases. Serum C-reactive protein determination on total 207 patients with infectious disease and allied conditions were done in the pediatric ward of Chungnnam National Hospital during the period from Jan, 1988... |
65 Cases of febrile convulsion were reviewed in terms of their clinical pictures and factors related to their recurrences. Seemingly related factors are: 1) age of first episode: The age of first ipisode was under 12months of age in 11.4% of initial cases and 46.7% of recurrent cases. 2) family history of convulsive disorder: There were family history of convulsive disorder in 23.4% of recurrent cases, compare to... |
The author analyzed the seizure types, clinical symptoms, and laboratory examinations in 156 epileptic children who were admitted to Maryknoll Hospital during the 6 years since June 1983 > The results were summarized as follows: 1) Of the 156 epileptic children, 48.1% exhibited generalized seizures, 37.2% partial seizures, 10. 2% unclassified seizures. The most common type was tonic-clonic seizure (37.8%). 2) Epilepsy was most frequent in children... |
The authors analyzed the causes, clinical manifestations, courses and outcomes in 29 children with status epilepticus who were admitted at Pusan National University Hospital between January 1980 and June 1989. The results were summarized as follows: 1) In sezure disorder, the incidence of status epilepticus was 7.1%. Status epilepticus was occured throughout childhood without age prevalence and the incidence male to female ratio was 3.1:1. 2) The causes... |
A prospective study was conducted to see the therapeutic effect of iron deficiency anemia on a different oral iron doses. Studied patients consisted of 48 children with iron deficiency anemia who were admitted to our Pediatric Department during January 1988 - September 1989. Three groups were consisted with Group A (element iron dose 3 mg/kg/d, 16 cases), Group B (3 mg/kg/d with vitamin C... |
To study the clinical characteristics and treatment result of childhood NHL, the retrospective study was performed on 82 children with NHL, experienced at the department of Pediatrics, Seoul National University Hospital, during 10 years from January 1979 to December 1988. The results were as follows; 1) The sex ratio of male to female was 2.4:1. 2) The age of patients ranged from 8 months to 15 years,... |
A clinical study was made on 558 cases of benign or malignant tumors occuring under the age of 16 years which had been observed at the National Medical Center during a period of 12 years, from January 1976 to December 1987. Five hundred fifty eight tumors were divided into 308 benign, 223 malignant and 27 uncertain tumors. The frequency of malignant tumors among total admitted... |
A rare form of congenital cystic lung disease, characterized by the presence of one or usually multiple interconnecting cyst, is called congenital cystic adenomatoid malformation of the lung. This disease almost invariably presents either in live premature or stillborn infants, and death in those infants bom alive usually occurs within a few hours of birth. Infants with congenital cystic adenomatoid malformation usually have tachypnea,... |
Congential pulmonary arteriovenous fistula is an uncommon malformation which has an abnormal connection between the pulmonary capillary bed, in which venous blood in the pulmonary artery is shunted through the fistula into the pulmonary vein without exposure to alveolar air, enters the left heart, and results in systemic arterial unsaturation, polycythemia, cyanosis and clubbing. Death often results from cerebral abscess and rupture of the... |
Transsphenoidal meningoencephalocele is congenital defects in the sphenoid bone through which meninges and brain tissue have herniated; the defect, located in the midline of the base of the skull, was first reported by Richter in 1813. The nine cases of transsphenoidal meningoencephalocele have been reported. Patients with transsphenoidal meningoencephalocele also may have other midline craniocerebral and midfacial anomalies, including additional meningoencephalocele hypertelorism, cleft palate, and abnormalities... |
The Dandy-Walker Syndrome is a developmental disorders of the brain characterized by cystic deformity of fourth ventricle, agenesis or hypoplasia of the cerebellar vermis, and hydrocephalus. This syndrome is frequently associated with central nervous system malformation and systemic anomalies. We experienced a case in a 2-day-old female who has multiple congenital anomalies. On physical examinations, macrocephaly with prominent occiput, encephalocele in the occipital area, microphth- almia,... |
In agenesis of the corpus callosum, the major nerve fiber tracts that connect the two carebral hemisphere are absent, and various associated anomalies involve almost all organs. We experienced a case of corpus callosum agenesis associated with situs ambiguus that has not been reported until now. A brief review of related literatures was done. |
Poland’s syndrome is a congenital disorder associated with absence of the pectoralis muscle and ipsilateral defect of the upper extremity, usually syndactyly. The syndrome is not hereditary and is of unknown origin. It affects males more frequently than females. Recently, we experienced a 1 year old male, who had the absence of right pectoralis muscle and ipsilateral syndactyly with hypoplasia of fingers. |
We experienced a case of aplastic anemia following hepatitis in a 4-year-old girl. Pancytopenia was developed during the convalescent period of hepatitis, and it was getting worse, while serial data of liver function test showed improvement. We tried a methylprednisolone pulse therapy, and about 7 months after treatment the CBC findings returned completely normal. She has enjoyed her healthy life during follow-up of over 2... |
Dermatomyositis is a rarely recognized disorder with poor prognosis. The mortality has been decreased after the initiation of steroid for ifs treatment. Authors experienced a case of der- matomyositis responded well to prednisone therapy and developed hyperglycemia laterly. A 14 year old boy was admitted to pediatric ward with the chief complaints of progressive muscular weakness and facial rash and diagnosed as having dermatomyositis... |