Skip Navigation
Skip to contents
Results by Year

View Wide

Filter

ARTICLE TYPE

PUBLICATION DATE

20 results
Display

Rare Cases of PLOD1-Related Kyphoscoliotic Ehlers-Danlos Syndrome in a Korean Family Identified by Next Generation Sequencing

Shin YL, Park YN, Jang MA

Kyphoscoliotic Ehlers-Danlos syndrome (kEDS) is an autosomal recessive connective tissue disorder characterized by muscular hypotonia, hyperextensible skin, skin fragility, joint hypermobility, and progressive kyphoscoliosis. The disorder results from a deficiency...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Ehlers-Danlos syndrome VIII with novel C1R variant accompanying white matter changes

Seo GH, Kim YM, Ghang B, Kim GH, Lee BH

Ehlers-Danlos syndrome (EDS) VIII is an autosomal dominant inherited connective tissue disorder characterized by intractable periodontal inflammation, absence of gingiva, pretibial plaques, skin hyperextensibility, joint hypermobility, and tissue fragility with...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Treatment of the wide open wound in the Ehlers-Danlos syndrome

Baik BS, Lee WS, Park KS, Yang WS, Ji SY

Ehlers-Danlos syndrome (EDS) is an inherited disorder of collagen biosynthesis and structure, characterized by skin hyperextensibility, joint hypermobility, aberrant scars, and tissue friability. Besides the skin, skeleton (joint) and vessels,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
The Vascular Type Ehlers-Danlos Syndrome Diagnosed after Delivery

Kim SM, Kang YD

Vascular Ehlers-Danlos sydrome (vEDS) is a life-threatening autosomal dominant inherited disorder of connective tissue characterized by arterial aneurysm, dissection and rupture, bowel rupture, and rupture of the gravid uterus. vEDS...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Ehlers-Danlos Syndrome in a Newborn Mistaken for Edwards Syndrome

Kim SK, An JW, Lee SH, Oh YK

The Ehlers-Danlos syndrome (EDS) is an inherited connective tissue disorder with special characteristics such as joint hypermobility, tissue fragility and skin abnormalities. The recently classification divide six subtypes. Dermatosparaxis types...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Spontaneous renal artery dissection in Ehlers-Danlos syndrome

Lim BH, Lee SI, Lim JH, Oh SJ, Chu MS, Ahn SH, Byun SJ

Primary dissection of the renal artery is rare. Spontaneous renal artery dissection can be associated with diseases such as medial degeneration, neurofibromatosis, syphilitic arteritis, tuberculosis, polyarteritis nodosa, Marfan syndrome, fibromuscular...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
[Secondary publication] Sudden Aortic Rupture in Ehlers-Danlos Syndrome Type IV

Baek T, Kim M, Ki CS, Park SH, Lee H, Kim KR, Choi BH

Ehlers-Danlos syndrome type IV (EDS IV) is a hereditary disorder of the connective tissue, characterized by easy bruising, thin skin with visible veins, and spontaneous rupture of the large arteries,...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Spontaneous Carotid-Cavernous Fistula in the Type IV Ehlers-Danlos Syndrome

Kim JG, Cho WS, Kang HS, Kim JE

Ehlers-Danlos syndrome (EDS) is a rare inherited connective disease. Among several subgroups, type IV EDS is frequently associated with spontaneous catastrophic bleeding from a vascular fragility. We report on a...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Anesthesia for a Cesarean Section in a Patient with Ehlers-Danlos Syndrome: A case report

Seo BS, Kim EJ, Lee JH, Lee SG, Ban JS, Min BW

Ehlers-Danlos syndrome (EDS) is an inherited connective tissue disorder characterized by skin hyperelasticity, joint hypermobility and tissue fragility. The clinical manifestations vary depending on the type of disease. Due to...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Type II and Classical Type Ehlers-Danlos Syndrome : Report of 3 Cases & Review of Korean Cases

Lee SY, Park SH, Choi HJ, Yun SK, Kim HU, Ihm CW

  • KMID: 2116190
  • Korean J Dermatol.
  • 2006 Jul;44(7):834-838.
Ehlers-Danlos syndrome (EDS) is a group of related conditions that commonly share the decrease of the tensile strength and integrity of the skin, joints and other tissues. We report three...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Dislocation of the Carpometacarpal Joint of the Thumb in Ehlers-Danlos Syndrome: A Case Report

Cheon SJ, Cho JY, Kang JH, Kim HT, Yoo CI

  • KMID: 2186830
  • J Korean Orthop Assoc.
  • 2005 Dec;40(7):1004-1008.
A subluxation or dislocation of the carpometacarpal joint of the thumb is a rare injury, which usually occurs from trauma. There is a relative dearth of literature about the results...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Classical Type Ehlers-Danlos Syndrome: Report of a Case and Review of Literature

Kwon HJ, Kim MY, Park YM, Kim HO

No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Ehlers-Danlos Syndrome Presenting with Neurological Symptoms

Jang YS, Park YH, Kim MK, Kim KS, Yoo KM, Suh KS

  • KMID: 2342848
  • J Korean Neurol Assoc.
  • 2000 Jul;18(4):515-517.
Ehlers-Danlos syndrome (EDS) is an inherited connective tissue disorder characterized by fragility of the skin, hyperelasticity of the skin, hyperextensible joints, vascular lesions, easy bruising, and excessive scarring after injuries....
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Type II Ehlers-Danlos Syndrome

Ha DJ, Park JY, Kim NI

  • KMID: 2303268
  • Korean J Dermatol.
  • 2000 Jul;38(7):997-998.
Ehlers-Danlos syndrome is a heterogeneous group of inherited generalized connective tissue disorders characterized by hyperextensibility and fragility of skin, joint hepermobility, abnormal scarring, easy bruisibility, visceral and neurological manifestations. It...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Surgical Treatment of Acute Type A Aortic Dissection in Ehlers-Danlos Syndrome

Jeong DS, Kim KH, Ahn H

  • KMID: 2062539
  • Korean J Thorac Cardiovasc Surg.
  • 2000 Nov;33(11):910-914.
Ehlers-Danlos syndrome type IV(the arterial-ecchymotic type) which has skin fragility, easy bruisability, and j oint hyperextensibility is occasionally combined with large vessel involve-ment and spontaneous catastrophic bleeding. As even a...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Type II Ehlers-Danlos Syndrome

Oh DH, Kim JK, Nam BD, Lee JE, Park JH

  • KMID: 2104468
  • J Korean Pediatr Soc.
  • 1999 Feb;42(2):268-273.
Ehlers-Danlos syndrome represents a group of inherited connective tissue disorders characterized by varying degrees of joint laxity, skin fragility and hyperextensibility, and a bleeding tendency. The essential defect is a...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Megabladder and Bladder Diverticulum Associated With Ehlers-Danlos Syndrome in Female

Boo MS, Choi CH, Choi HC, Min KS, Choi SH

  • KMID: 2290185
  • Korean J Urol.
  • 1996 Jun;37(6):714-717.
The Ehlers-Danlos syndrome is a congenital anomaly having collagen metabolism with clinical and genetic heterogeneity. It has been classified into ten distinct clinical forms. Urinary bladder diverticula associated with Ehlers-Danlos...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A case of type VI Ehlers-Danlos syndrome

Pai KS, Chung YM, Namgung R, Lee C, Han DG

  • KMID: 1691574
  • J Korean Pediatr Soc.
  • 1991 Dec;34(12):1717-1723.
No abstract available.
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
A Case of Ehlers-Danlos Syndrome Accompanied by Mitral Valvular Prolapse and Atrial Septal Defect

Kim JW, Jung IS, Lim KS, Choi YM, Choi JC, Ohk JH, Shu DR

Ehlers-Danlos Syndrome(EDS) is an inherited disorder of the connective tissue disease that is usually transmitted as autosomal dominant trait. The defect in the biogenesis of collagen results in varying degree...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close
Ehlers-Danlos Syndrome: 2 Cases Report

Lee YS, Yang HS, Cho YW

The Ehlers-Danlos syndrome is a familial disorder of connective tissue, and seven distinct clinical forms are reported. Author experienced two cases of the type 3 Ehlers-Danlos syndrome which present hypermobility...
CITED
export Copy
Close
SHARE
Twitter Facebook
Close

Go to Top

Copyright © 2021 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr