http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
Roh, Eui Jung,Lim, Jae Woo,Ko, Kyoung Og,Cheon, Eun Jung KOREAN ACADEMY OF MEDICAL SCIENCE 2007 JOURNAL OF KOREAN MEDICAL SCIENCE Vol.22 No.2
<P>Childhood obesity seems to contribute to the development of vascular inflammation and the progression of arterial wall changes. High-sensitivity C-reactive protein (hs-CRP) has recently emerged as a useful biomarker for vascular inflammation associated with atherosclerosis. The objectives of this study were to evaluate the association of the serum hs-CRP level with ultrasonic findings of early atherosclerosis, carotid intima-media wall thickness (IMT) and brachial flow-mediated dilation (FMD), in obese children. Thirty eight obese children and 45 sex/age-matched healthy control children were recruited. Serum CRP levels were measured by the high-sensitive latex turbidimetric immunoassay, and we measured carotid IMT and brachial FMD using high-resolution B-mode ultrasonography. Obese children had significantly higher hs-CRP levels (1.40±0.74 mg/L vs. 0.55±0.49 mg/L, <I>p</I><0.01), as well as increased IMT (0.52±0.09 mm vs. 0.41±0.07 mm, <I>p</I><0.01) and impaired FMD (7.35±7.78% vs. 20.34±16.81%, <I>p</I><0.01) compared to healthy controls. Serum hs-CRP correlated positively with IMT (r=0.413, <I>p</I><0.05) and inversely with FMD (r=-0.350, <I>p</I><0.05) in the obesity group. Measurement of the serum hs-CRP level is a simple, cheap, and highly reproducible assay and correlates with IMT and FMD in obese children. Thus, it would be a useful marker for evaluating and estimating the degree of atherosclerosis in children.</P>
대뇌 피질의 이형성과 소뇌 위축 소견이 동반된 Seckel 증후군 1례
윤장원(Jang Won Yoon),임재우(Jae Woo Lim),천은정(Eun Jung Cheon),고경옥(Kyoung Og Ko),이영혁(Young Hyuk Lee) 대한소아신경학회 2007 대한소아신경학회지 Vol.15 No.1
Seckel 증후군은 드문 상염색체 열성 질환으로 새와 같은 머리 및 저신장과 소두증을 특징으로 한다. 정신지체를 동반하며 뇌 자기공명영상을 통해 중추 신경계의 이상을 확인할 수 있다. 저자들은 특징적인 외모와 저신장, 소두증, 지능 저하를 보여 Seckel 증후군으로 진단된 환아에서 뇌 자기공명영상을 통해 대뇌 피질의 이형성과 소뇌의 위축소견을 포함하는 중추신경계 이상을 확인하였으며 국내에서는 이에 대한 보고가 없어 문헌 고찰과 함께 보고하는 바이다. Seckel syndrome is a rare autosomal recessive disease. The characteristic features of Seckel syndrome include Intrauterine and postnatal growth deficiency, severe microcephaly, and a bird-like head. General appearance of our patient was characterized by Pre- and postnatal growth retardation, microcephaly, large eye, and a beaked nose. The patient had mental retardation with CNS anomalies. The CNS anomalies seen in the patient included cerebral dysgenesis and cerebellar atrophy. So, we report the case of CNS anomalies in Seckel syndrome.