• 대한음성언어의학회:학술대회논문집
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• 대한음성언어의학회 2006년도 제25회 학술대회
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• pp.152-152
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• 2006

• Clinical and Experimental Pediatrics
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• 제49권10호
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• pp.1026-1030
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• 2006

Mental retardation(MR) is one of the most common developmental disabilities, which is characterized by deficits in intellectual and adaptive functions. Most children with MR have cognitive limitation in the mild range. With respect to the etiology, it is believed that genetic and environmental factors are interrelated and show variable pictures. Most children with MR present with speech and language delay during the early years. The diagnosis can be made by clinical features and neuropsychological tests of intelligence and adaptive functioning. The treatment is limited, but many associated problems are amenable to multidisciplinary interventions. The article will review the recent advances in the management of MR and other neurodevelopmental disorders in children.

• 대한치과의사협회지
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• 제53권11호
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• pp.779-788
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• 2015

Individuals with special needs include those with behavioral issues, developmental disorders, cognitive disorders, congenital or genetic disorders, or systemic disease. These conditions may place them at increased risk for oral diseases. Dental management of patients with special needs require in-depth understanding of the background of disability and available behavioral guidance theories. Therefore dental team members need more training in the theory and practice of behavior management principles, which might lead to a clinical experience that is more respectful of the dignity and independence of patients with special needs. The dental professional should be flexible to modify the behavior management approach according to the individual patients needs. Also a family/care-giver centered approach based on their preferences and concerns, the patient's challenging behaviors, and related medical problem can serve to improve the treatment planning and oral health management of dental patients with special needs. This article focuses on uncooperative behavior and behavior management, which help practicing dentists to understand their role in the care of patients with special needs.

• Clinical and Experimental Pediatrics
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• 제62권4호
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• pp.126-130
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• 2019

Purpose: In this meta-analysis, relevant case-control and cohort studies were pooled to evaluate the association between preeclampsia and the risk of autism spectrum disorders (ASDs) in children. Methods: A search for relevant studies in major databases, including Web of Science, PubMed, and Scopus, was performed up to May 2018. The odds ratios (ORs) or rate ratios (RRs) with 95% confidence intervals (CIs) were extracted from eligible studies to determine the association among studies. Results: The pooled estimates of ORs and RRs indicated a significant association between preeclampsia and ASD [(OR, 1.36; 95% CI, 1.12-1.60) and (RR, 1.30; 95% CI, 1.20-1.41)]. Conclusions: Despite existing controversy, our findings indicated that preeclampsia was associated with an increased risk of ASD among children.

• Molecules and Cells
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• 제42권6호
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• pp.441-447
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• 2019

RAS gene mutations are frequently found in one third of human cancers. Affecting approximately 1 in 1,000 newborns, germline and somatic gain-of-function mutations in the components of RAS/mitogen-activated protein kinase (RAS/MAPK) pathway has been shown to cause developmental disorders, known as RASopathies. Since RAS-MAPK pathway plays essential roles in proliferation, differentiation and migration involving developmental processes, individuals with RASopathies show abnormalities in various organ systems including central nervous system. The frequently seen neurological defects are developmental delay, macrocephaly, seizures, neurocognitive deficits, and structural malformations. Some of the defects stemmed from dysregulation of molecular and cellular processes affecting early neurodevelopmental processes. In this review, we will discuss the implications of RAS-MAPK pathway components in neurodevelopmental processes and pathogenesis of RASopathies.

• Journal of the Korean Academy of Child and Adolescent Psychiatry
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• 제10권1호
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• pp.64-75
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• 1999

본 연구에서는 전반적 발달장애 pervasive developmental disorder(이하 PDD)의 공존질환과 동반증상의 현황을 파악하고자 전반적 발달장애 아동에서의 동반증상과 공존질환의 빈도 및 특성을 알아보고 발달성 언어장애 developmental language disorder(이하 DLD)와의 차이를 비교해 보았다. 연구대상은 1996년 1월부터 1999년 3월까지 국립서울정신병원 소아정신과 외래에서 통원치료를 받았거나 발달장애 주간치료프로그램에 참가했던, DSM-IV를 기준으로 소아정신과 전문의에 의해 진단된, 만 1세에서 11세 아동 352명 이었으며 이중 PDD는 209명(남179, 여30), DLD는 143명(남119, 여24)이었다. 진단적 평가에는 병록지, 언어평가, 작업평가, 가정방문보고서, 부모양육보고서, SMS, CARS, PEP 결과 등을 참조하였다. 진단군에 따른 각각에서의 공존질환과 동반증상의 빈도와 특징을 비교분석하였고, PDD아동 64명을 CARS에 따라 3군으로 나누어 동반증상의 양상을 비교하였으며, 106명을 대상으로 각 동반증상과 교육진단검사 소항목과의 관계를 검증하였다. 연구결과 PDD와 DLD 양군에서 공존질환의 비율은 각각 19.6%, 41.2%이었고, 동반증상 13개 항목의 평균 동반비율은 31.47%, 22.13%이었다. 비정상적 집착, 강박증, 자해행동, 상동증, 수면문제, 기묘한 반응 등은 PDD에서 유의하게 높은 빈도를 보였다. 동반비율에서 PDD에서는 비정상적 집착, 상동증, 주의집중 부족, 부적절한 정서 등의 순서를 보인 반면, DLD에서는 주의집중 부족, 공격성, 부적절한 정서, 행동과다, 비정상적 집착 등의 순서를 보였다. 각 동반증상의 유무에 따른 교육진단검사 소항목 들의 양상을 분석해본 결과, 전체군에서는 비정상적 집착, 자기자극행동, 상동증, 부적절한 정서, 수면문제, 기묘한 반응 등의 유무에 따라 유의한 차이를 보였고, 진단별에 따라서는 두 군 모두 차이를 나타낸 항목이 없었다. 한편 CARS에 따라 유의한 차이를 보인 동반증상은 상동증, 불안, 수면문제 등이었다. 이와 같은 결과는 전반적 발달장애에서의 공존질환 및 동반증상의 임상적 중요성을 나타내며, 추후 공존질환과 동반증상의 빈도 및 특성에 따라 세부적인 진단과 이에 따른 현실적인 치료적 접근이 필요함을 시사한다.

• Clinical and Experimental Pediatrics
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• 제45권10호
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• pp.1199-1203
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• 2002

목 적: 언어발달장애를 주소로 내원하는 소아들을 대상으로 청성뇌간반응(ABR)을 선별검사로 시행함으로써 그 원인을 조기 발견하고 조기 치료함으로써 이들의 장애를 최소화하고 언어발달 과정에 도움을 주고자 본 연구를 시행하였다. 방 법 : 1999년 1월부터 2001년 12월까지 3년 동안 경북대학교병원 소아과에 언어발달장애를 주소로 내원한 18개월 이상 소아 139례를 대상으로 하여 청성뇌간반응(ABR)을 시행하였으며 이들의 임상진단과 ABR 이상에 따라 분류하였다. 결 과 : 전체 139례 중 ABR 검사상 이상소견을 보인 환아는 15례(10.8%)였으며 전반적 발달장애 7례, 발달성 언어장애 4례, 기타 4례로 나타났으며 이상소견을 보인 환아 중 7례는 전음성 난청이었으며 8례는 감각신경성 난청이었다. 또한 ABR 검사상 정상을 보인 18개월에서 7세 사이의 I파 및 V파의 평균잠복기 및 표준편차는 각각 $1.40{\pm}0.13$, $5.57{\pm}0.26$이었으며, I-V의 정점간 잠복기는 $4.18{\pm}0.24$였다. 중등도 이상의 감각신경성 난청환아의 4례에서 보청기를 착용하였으며 이들을 추적 관찰하였다. 결 론: 언어발달장애를 주소로 내원하는 소아들에게 선별검사로서의 ABR은 반드시 필요한 것으로 생각되며 이것을 통해 감각신경성 난청을 조기 발견하고 감각 신경성 난청의 경우 보청기를 사용하여 조기 치료함으로써 이들의 신경학적 발달 및 사회적 적응에 도움을 줄 수 있을 것이다.

• Clinical and Experimental Pediatrics
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• 제63권11호
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• pp.438-446
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• 2020

Background: Most developmental screening tools in Korea are adopted from foreign tests. To ensure efficient screening of infants and children in Korea, a nationwide screening tool with high reliability and validity is needed. Purpose: This study aimed to independently develop, standardize, and validate the Korean Developmental Screening Test for Infants and Children (K-DST) for screening infants and children for neurodevelopmental disorders in Korea. Methods: The standardization and validation conducted in 2012-2014 of 3,284 subjects (4-71 months of age) resulted in the first edition of the K-DST. The restandardization and revalidation performed in 2015-2016 of 3.06 million attendees of the National Health Screening Program for Infants and Children resulted in the revised K-DST. We analyzed inter-item consistency and test-retest reliability for the reliability analysis. Regarding the validation of K-DST, we examined the construct validity, sensitivity and specificity, receiver operating characteristic curve analysis, and a criterion-related validity analysis. Results: We ultimately selected 8 questions in 6 developmental domains. For most age groups and each domain, internal consistency was 0.73-0.93 and test-retest reliability was 0.77-0.88. The revised K-DST had high discriminatory ability with a sensitivity of 0.833 and specificity of 0.979. The test supported construct validity by distinguishing between normal and neurodevelopmentally delayed groups. The language and cognition domain of the revised K-DST was highly correlated with the K-Bayley Scales of Infant Development-II's Mental Age Quotient (r=0.766, 0.739), while the gross and fine motor domains were highly correlated with Motor Age Quotient (r=0.695, 0.668), respectively. The Verbal Intelligence Quotient of Korean Wechsler Preschool and Primary Scales of Intelligence was highly correlated with the K-DST cognition and language domains (r=0.701, 0.770), as was the performance intelligence quotient with the fine motor domain (r=0.700). Conclusion: The K-DST is reliable and valid, suggesting its good potential as an effective screening tool for infants and children with neurodevelopmental disorders in Korea.

• 수면정신생리
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• 제2권1호
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• pp.13-22
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• 1995

To provide the physician with adequate information to diagnose and treat sleepwalking and sleep terrors, the author reviewed clinical features, epidemiology, causative and precipitating factors, polysomnography, diagnosis, differential diagnosis, and treatment for these disorders. Sleepwalking and sleep terrors have been defined as disorders of arousal that occur early in the night and have their onset during stage 3 or 4 sleep. In both disorders, patients are difficult to arouse, and complete amnesia or minimal recall of the episode is frequent. Genetic, developmental, and psychological factors have been identified as causes of both sleepwalking and sleep terrors. Sleepwalking and sleep terrors typically begin in childhood or early adolescence and are usually outgrown by the end of adolescence. When sleepwalking or sleep terrors have a post-pubertal onset or continue to adulthood, psychopathology is a more significant causative factors. The behavior that occur from deep slow-wave sleep can be painful or dangerous to the individual and/or disturbing to those close to that individual. The assessment of patients suspected of having these conditions requires a thorough medical and sleep history. The most important consideration in managing patients with sleepwalking or sleep terrors episodes is protection from injury.

• Journal of Yeungnam Medical Science
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• 제39권1호
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• pp.58-61
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• 2022

Mega cisterna magna (MCM), one of the members of the Dandy-Walker complex, is a developmental malformation of the posterior fossa that is larger than 10 mm but morphologically does not affect the vermis and cerebellar hemispheres. Reports of psychiatric disorders associated with this anomaly are rare. We present the case of a patient with MCM who presented with a psychotic manic attack and was diagnosed with bipolar disorder. A 28-year-old female, single housewife, university graduate, presented with irritability, decreased sleep and appetite, distraction, and agitation. The patient also had a delusion of reference. In the clinical follow-up, an increase in energy and an increase in the amount of speech were observed. Her neurological examination was normal, and cranial magnetic resonance imaging revealed an MCM. The relationship and clinical significance of MCM with psychosis and mood disorders have not yet been fully elucidated. It is not known whether this association is accidental or based on etiological commonality. The purpose of this case report is to review the relationship between the cerebellum and psychiatric symptoms and to contribute to the literature.