Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

more+
SELECT FILTER
 
Close

PUBLICATION DATE

51 results
Display

Minimally Invasive Mitral Valve Repair in a Woman with Marfan Syndrome and Type B Dissection

Lim MH, Je HG, Lee SK

We report the case of a patient with mitral regurgitation complicated by type B dissection and Marfan syndrome (MFS) who was managed successfully with minimally invasive mitral valve repair. Without...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Atypical Neonatal Marfan Syndrome with p.Glu1073Lys Mutation of FBN1: the First Case in Korea

Heo JS, Song JY, Choi EY, Kim EH, Kim JH, Park SE, Jeon JH

Neonatal Marfan syndrome (nMFS) is considered to be on the most severe end of the spectrum of type I fibrillinopathies. The common features of nMFS include ascending aortic dilatation, severe...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Femur Neck Fracture in a Young Marfan Syndrome Patient

Kwon YU, Kong GM, Park JH

Marfan syndrome is an autosomal dominant and could decrease bone mineral density. So patients with Marfan syndrome could vulnerable to trauma in old ages. We present the first report, to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Clinical Characteristics of Marfan Syndrome in Korea

Lim AY, Song JS, Kim EK, Jang SY, Chung TY, Choi SH, Sung K, Huh J, Kang IS, Choe YH, Ki CS, Kim DK

BACKGROUND AND OBJECTIVES: Marfan syndrome (MFS) is a connective tissue disorder with autosomal dominant inheritance and a highly variable clinical spectrum. However, there are limited data available on the clinical...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A novel FBN1 gene mutation associated with early-onset pneumothorax in Marfan syndrome

Park MJ, Lee DH, Shin YL, Hong YH

Marfan syndrome (MFS) is an inherited connective tissue disorder with a mutation in the fibrillin-1 (FBN1) gene. Fibrillin is a major building block of microfibrils, which constitute the structural component...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Infantile Marfan syndrome in a Korean tertiary referral center

Seo YJ, Lee KE, Kim GB, Kwon BS, Bae EJ, Noh CI

PURPOSE: Infantile Marfan syndrome (MFS) is a rare congenital inheritable connective tissue disorder with poor prognosis. This study aimed to evaluate the cardiovascular manifestations and overall prognosis of infantile MFS...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Stanford type A aortic dissection in a patient with Marfan syndrome during pregnancy: a case report

Kim WH, Bae J, Choi SW, Lee JH, Kim CS, Cho HS, Lee SM

Aortic dissection during pregnancy is a devastating event for both the pregnant woman and the baby. We report a case of acute aortic dissection (Stanford type A) in a pregnant...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Surgical Management of Mitral Regurgitation in Patients with Marfan Syndrome during Infancy and Early Childhood

Kim ER, Kim WH, Choi ES, Cho S, Jang WS, Kim YJ

BACKGROUND: Mitral regurgitation is one of the leading causes of cardiovascular morbidity in pediatric patients with Marfan syndrome. The purpose of this study was to contribute to determining the appropriate...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Marfan syndrome and symptomatic dural ectasia: A case report and literature review

Eom SN, Kim DC, Kim KN, Kim SH

Dural ectasia refers to the widening or ballooning of the dural sac surrounding the spinal cord. It can affect any plane of the spinal canal, but occurs primarily in the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Inadequate spinal anesthesia in a parturient with Marfan's syndrome due to dural ectasia

Yang HJ, Baek IC, Park SM, Chun DH

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Significant fibrosis after radiation therapy in a patient with Marfan syndrome

Suarez EM, Knackstedt RJ, Jenrette J

Marfan syndrome is one of the collagen vascular diseases that theoretically predisposes patients to excessive radiation-induced fibrosis yet there is minimal published literature regarding this clinical scenario. We present a...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Acute Aortic Dissection in Pregnancy with the Marfan Syndrome

Kim SW, Kim D, Hong JM

  • KMID: 2288796
  • Korean J Thorac Cardiovasc Surg.
  • 2014 Jun;47(3):291-293.
Acute aortic dissection (AAD) during pregnancy can be fatal to both the pregnant mother and the baby, particularly in patients with the Marfan syndrome. We report a case of the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Analysis of Disease Progression-Associated Gene Expression Profile in Fibrillin-1 Mutant Mice: New Insight into Molecular Pathogenesis of Marfan Syndrome

Kim KL, Choi C, Suh W

  • KMID: 2170654
  • Biomol Ther.
  • 2014 Mar;22(2):143-148.
Marfan syndrome (MFS) is a dominantly inherited connective tissue disorder caused by mutations in the gene encoding fibrillin-1 (FBN1) and is characterized by aortic dilatation and dissection, which is the...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
General Anesthesia for Dental Treatment of a Pediatric Patient with Marfan Syndrome

Kim KJ, Bak S, Hyun HK, Shin TJ, Kim JW

Multiple caries in a pediatric patient often requires dental treatment under general anesthesia, especially when the patient is suffering from a systemic disease. The patient was a 6-year-old boy with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case Report of Acute Type II Aortic Dissection in a Patient with Marfan's Syndrome and Who Was 24 Weeks Pregnant: A case report

Hwang UD, Chung CH, Ryu YG, Lim J

  • KMID: 1885751
  • Korean J Thorac Cardiovasc Surg.
  • 2007 Jul;40(7):508-511.
The causes of aortic dissection are usually hypertension, connective tissue disease such as Marfan syndrome, congenital valvular abnormality such as bicuspid aortic valve, iatrogenic injury, pregnancy and drugs. Previous studies...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Annular Plication Technique to Facilitate Sliding Annuloplasty in a Marfan's Syndrome Patient

Je HG, Lee JW

  • KMID: 2062864
  • Korean J Thorac Cardiovasc Surg.
  • 2007 Jun;40(6):441-444.
Sliding annuloplasty has been used for mitral valve repair in conjunction with posterior leaflet quadrangular resection to avoid systolic anterior motion of the anterior leaflet of the mitral valve. Herein,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Abdominal Aortic Aneurysm in Marfan's Syndrome: Two Cases

Kim JH, Kim TH, Park SC, Won YS, Yun SS, Moon IS, Park JS, Kim SN, Koh YB

  • KMID: 1941004
  • J Korean Soc Vasc Surg.
  • 2006 May;22(1):30-34.
Marfan syndrome is an inherited autosomal dominant disorder of the connective tissues, and the afflicted patients present with abnormalities of the skeletal, ocular, and cardiovascular system. The progressive dilatation of...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Identification of Molecular Defects in Korean Patients with Marfan Syndrome

Shin MS, Park HY, Lim Y, Shin GJ, Jang Y, Jang BC, Chung N

BACKGROUND AND OBJECTIVES: Marfan syndrome is an autosomal dominant heritable disease of connective tissue which is characterized by cardinal features mainly in the cardiovascular, ocular and skeletal systems. Aneurysms or...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The Visual Prognosis in Marfan Syndrome with Ectopia Lentis

Yang JW, Kim HS, Lee YC

  • KMID: 2206197
  • J Korean Ophthalmol Soc.
  • 2002 Oct;43(10):1876-1881.
PURPOSE: To assess the clinical characteristics, indications of operation, operative methods and visual prognosis in Marfan syndrome with ectopia lentis. METHODS: Medical records of 13 patients (24 eyes) operated due to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Combined Repair of Pectus Excavatum and Open Heart Surgery in Marfan's Syndrome

Shin JK, Jung JP, Lee YJ

  • KMID: 1916142
  • Korean J Thorac Cardiovasc Surg.
  • 2002 Jul;35(7):556-559.
The presense of pectus excavatum in Marfan's syndrome may complicate cardiac operation by making midline sternotomy technically more difficult and limiting the operative exposure of the heart. We operated on...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2022 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr