http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
이성구,이소연,임소희,유기동,백상홍,김철민,최규보 대한내과학회 2003 대한내과학회지 Vol.65 No.1
LEOPARD 증후군은 흑자와 심장기형을 동반하는 비교적 드문 임상 증후군으로 심전도 이상, 양안 격리증, 폐동맥 협착, 비뇨생식기 기형, 성장지연, 감각신경성 청력장애 등 다양한 임상 증상을 보인다. 본 저자들은 흑자증, 양안 격리증, 심전도상 우각차단, 삼심방 등을 동반한 LEOPARD 증후군을 경험하였기에 문헌고찰과 함께 보고하는 바이다. The LEOPARD syndrome is an acronym and serves as a mnemonic for the features of this autosomal dominant syndrome : L - lentigines (multiple), E - electrocardiographic conduction abnormalities, O - ocular hypertelorism, P - pulmonary stenosis, A - abnormalities of genitalia, R - retardation of growth, and D - deafness (sensoryneural). The main features of the syndrome are multiple lentigines in combination with congenital heart malformations. These frequently accompanied cardiac abnormalities are pulmonary stenosis, hypertrophic cardiomyopathy, and various ECG abnormalities. It is advisable to make cardiac evaluation in a patient with LEOPARD syndrome in spite of no clinical symptoms or signs, since cardiac dysfunction may be progressive or developed later. We experienced a case of this syndrome in a 31 year-old female, presenting multiple lentigines, ocular hypertelorism, and congenital cardiac abnormalities of incomplete right bundle branch block and cor triatriatum. We report the case with brief literature review.