1.Genetic Neurological Disorders in Childhood.
Journal of the Korean Pediatric Society 2003;46(Suppl 2):S319-S329
No abstract available.
Nervous System Diseases*
2.Overview of Epileptogenisis.
Journal of the Korean Child Neurology Society 2001;9(1):192-200
No abstract available.
3.Subacute and Chronic Encephalitis in Children : Etiologies and Clinical Manifestations.
Journal of the Korean Medical Association 1997;40(7):828-834
No abstract available.
Child*
;
Encephalitis*
;
Humans
4.Risk factors in fullterm children with cerebral palsy.
Journal of the Korean Child Neurology Society 1993;1(1):41-49
No abstract available.
Cerebral Palsy*
;
Child*
;
Humans
;
Risk Factors*
5.Action Mechanisms of Anticonvulsants.
Journal of the Korean Child Neurology Society 2001;9(2):255-268
No abstract available.
Anticonvulsants*
6.A case of infantile hemifacial spasm.
Journal of the Korean Child Neurology Society 1993;1(2):156-159
No abstract available.
Hemifacial Spasm*
7.Clinical Investigation of Childhood Epilepsy.
Yeungnam University Journal of Medicine 1985;2(1):103-111
Childhood epilepsy which has high prevalence rate and inception rate is one of the commonest problem encountered in pediatrician. In contrast with epilepsy of adult, in childhood epilepsy, more variable and varying manifestations are found because the factors of age, growth and development exert their influences in the manifestations and the courses of childhood epilepsy. Moreover epilepsy children have associated problems such as physical and mental handicaps, psychological disorders and learning disability. For these reasons pediatrician who deals with epileptic children experiences difficulties in making diagnosis and managing them. In order to improve understanding and management of childhood epilepsy, authors reviewed 103 cases of epileptic patients seen at pediatric department of Yeungnam University Hospital retrospectively. The patients were classified according to the type of epileptic seizure. Suspected causes of epilepsy, associated conditions of epileptic patients, age incidence and the findings of brain CT were reviewed. Large numbers of epileptic patients (61.2%) developed their first seizures under the age of 5. The most frequent type of epileptic seizure was generalized tonic-clonic, tonic, clonic seizure (49.5%), followed by simple partial seizure with secondary generalization (17.5%), simple partial seizure (7.8%), atypical absence (5.8%) and unclassified seizure (5.8%). In 83.5% of patients, we could not find specific cause of it, but in 16.5% of cases, history of neonatal hypoxia (4.9%), meningitis (3.9%), prematurity (1.9%), small for gestational age (1.0%), CO poisoning (1.0%), encephalopathy (1.0%) were found. 30 cases of patients had associated diseases such as mental retardation, hyperactivity, delayed motor milestones or their combinations. The major abnormal findings of brain CT performed in 42 cases were cortical atrophy, cerebral infarction, hydrocephalus and brain swelling. This review stressed better designed classification of epilepsy is needed and with promotion of medical care, prevention of epilepsy is possible in some cases. Also it is stressed that childhood epilepsy requires multidisciplinary therapy and brain CT is helpful in the evaluation of epilepsy with limitation in therapeutic aspects.
Adult
;
Anoxia
;
Atrophy
;
Brain
;
Brain Diseases
;
Brain Edema
;
Cerebral Infarction
;
Child
;
Classification
;
Diagnosis
;
Epilepsy*
;
Generalization (Psychology)
;
Gestational Age
;
Growth and Development
;
Humans
;
Hydrocephalus
;
Incidence
;
Intellectual Disability
;
Learning Disorders
;
Meningitis
;
Poisoning
;
Prevalence
;
Retrospective Studies
;
Seizures
8.The Relationship between Underlying Diseases and the Patterns of Abnormal MR Image Findings in Childhood White Matter Diseases .
Journal of the Korean Child Neurology Society 2003;11(1):111-119
PURPOSE: In children disorders affecting brain white matter are not uncommon and MRI has high sensitivity to detect white matter lesions. We performed this study to find out the distribution of underlying diseases that show abnormal white matter image findings on brain MRI and the relationship between the underlying diseases and some particular patterns of MR imaging abnormalities. METHODS: Out of 1477 pediatric patients who visited the department of pediatrics of Yeungnam University Medical Hospital and took brain MRIs from January 1995 to June 2001, ninety five patients with white matter abnormalities on T2 MR images were evaluated retrospectively. This study excluded the patients with brain tumor, brain abscess, trauma, secondary white matter abnormalities due to hydrocephalus, cerebral infarct, and those whose main lesions were gray matter. RESULTS: The most common underlying disease was cerebral palsy(50 cases, 52.6%), followed by acute disseminated encephalitis(10 cases, 10.5%), intrauterine CMV infections (9 cases, 9.5%), inherited neurometabolic disorders(7 cases, 7.4%). In 12 patients(12.6%) with some neurological problems such as afebrile seizures and developmental delay, no underlying disease were found. The most common pattern of abnormal image findings was periventricular white matter lesions(45.3%) strongly related with cerebral palsy. The pattern of peritrigonal deep white matter lesions was found in 19 patients(20.0%), in 10 patients of whom no underlying diseases were found. The pattern of multiple round margined scattered lesions was found in all the 10 patients(10.5%) of acute disseminated encephalitis. CONCLUSION: There are diverse underlying diseases showing abnormal white matter image findings on MR in pediatric patients and particular patterns of abnormal image findings may serve to make a specific diagnosis possible. But not in a small group of children no diagnosis was established. Further studies regarding the underlying diseases affecting white matter lesions and more detailed knowledge of abnormal MR image findings are needed.
Brain
;
Brain Abscess
;
Brain Neoplasms
;
Cerebral Palsy
;
Child
;
Diagnosis
;
Encephalitis
;
Humans
;
Hydrocephalus
;
Leukoencephalopathies*
;
Magnetic Resonance Imaging
;
Pediatrics
;
Retrospective Studies
;
Seizures
9.The Acute Intermittent Peritoneal Dialysis in Acute Renal Failure of Newborn and Young Infants.
Yeungnam University Journal of Medicine 1986;3(1):375-382
We studied the effects of the acute intermittent peritoneal dialysis in severe acute renal failure of 1 newborn infant and 2 young infants during 18 months period from February 1985 to April 1986. The predisposing illnesses were severe acute gastroenteritis with dehydration. Reye's syndrome, and bilateral nephrolithiasis with hyperuricemia. The concomitant illnesses were severe hypernatremia, hyponatremia, hyperkalemia, hypocalcemia, hypoglycemia, DIC (disseminated intravascular coagulopathy). Paralytic ileus, metabolic acidosis and gastrointestinal bleeding. As a dialysate, Imperinol solutionR, 1.5% was used in all cases. The cycles of dialysis were 8, 16, and 41 times in each cases. Observed complications during dialysis were leakage, and abdominal wall and scrotal swelling in 2 cases, hyperglycemia in 1 case, and peritonitis in 1 case. Acinetobacter calcoaceticus was cultured in peritoneal fluid of peritonitis. These complications were treated by stopping dialysis in leakage and abdominal wall swelling, insulin therapy in hyperglycemia, and intraperitoneal and systemic antibiotics therapy in peritonitis. We experienced improvements of severe acute renal failure with variable concomitant illnesses by acute intermittent peritoneal dialysis despite of the treatable complications of dialysis in all cases.
Abdominal Wall
;
Acidosis
;
Acinetobacter calcoaceticus
;
Acute Kidney Injury*
;
Anti-Bacterial Agents
;
Ascitic Fluid
;
Dacarbazine
;
Dehydration
;
Dialysis
;
Gastroenteritis
;
Hemorrhage
;
Humans
;
Hyperglycemia
;
Hyperkalemia
;
Hypernatremia
;
Hyperuricemia
;
Hypocalcemia
;
Hypoglycemia
;
Hyponatremia
;
Infant*
;
Infant, Newborn*
;
Insulin
;
Intestinal Pseudo-Obstruction
;
Nephrolithiasis
;
Peritoneal Dialysis*
;
Peritonitis
;
Reye Syndrome
10.A clinical study on children with delayed language development.
Jeong Ho KIM ; Han Ku MOON ; Jeong Ok HAH
Yeungnam University Journal of Medicine 1991;8(2):24-34
Delayed emergence of speech or language are frequent causes for concern about development during early childhood. Delay in evaluation and proper management until school entry in more likely to result in frustration, anxiety and school failure. Many language disturbances and their attendant behavior disorders respond to intensive language therapy. Authors analyzed the medical records of 52 children with delayed language development evaluated during 30 months from January 1986 through June 1988. The results were as follows: 1. The majority of cases were evaluated at the age of 2-2.9 year old (16 cases, 30.8%) and 3-3.9 year old (11 cases, 21.2%) 2. Male to female ratio was 3:1 3. The most common cause was mental retardation (53.8%), followed by developmental language disorder (23.1%) and autism (13.5%) 4. The most common associated condition was dysarticulation (17.3%), followed by strabismus (9.6%) and seizures (7.7%) 5. Special education was recommended in cases of 23 (44.2%), speech therapy in 12 cases (23.1%) and consultation to child psychiatry in 7 cases (13.5%) Making diagnosis of underlying disorders in not simple because assessment of intelligence in young children in difficult and only a few tests are standardized. More detailed study on children with delayed language development and development of psychometric tests for handicapped children are necessary, especially in Korea.
Anxiety
;
Autistic Disorder
;
Child Psychiatry
;
Child*
;
Clinical Study*
;
Diagnosis
;
Disabled Children
;
Education, Special
;
Female
;
Frustration
;
Humans
;
Intellectual Disability
;
Intelligence
;
Korea
;
Language Development Disorders
;
Language Development*
;
Language Therapy
;
Male
;
Medical Records
;
Mental Disorders
;
Psychometrics
;
Seizures
;
Speech Therapy
;
Strabismus