Literature DB >> 7206598

Case report and study of collagen metabolism in Marfan's syndrome.

R Halbritter, M Aumailley, R Rackwitz, T Krieg, P K Müller.   

Abstract

The case report on a 33 year old woman with prominent features of Marfan's syndrome is presented. Characteristic signs were seen in the bones, the eyes, the cardiovascular system, and the lungs. Due to regurgitation of both the aortic and mitral valves and an aneurysm of the ascending aorta a double valve replacement was made, including a prosthesis of the aorta. The problems of early diagnosis and therapy of the life-threatening cardiovascular complications are discussed. Tissue specimens from the aorta were analysed histochemically and biochemically. Histology showed a typical necrosis of the media with cyst formation. Biochemical analysis by in vitro labeling of collagen in tissue explants and by electron microscopical evaluation showed proportions of type I and type III collagen which were significantly different from controls. In both the media and the adventitia the amount of type I collagen was drastically reduced as shown by quantitation of collagen and procollagen. Fibroblasts derived from the skin of the patient showed a normal content of type I and type III collagen. It is conceivable that the reduced content of type I collagen in the aortic wall is responsible for the weakness of the vessel wall causing formation of aneurysm and its sequelae.

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Year:  1981        PMID: 7206598     DOI: 10.1007/bf01477287

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  33 in total

1.  The cardiovascular aspects of Marfan's syndrome: a heritable disorder of connective tissue.

Authors:  V A McKUSICK
Journal:  Circulation       Date:  1955-03       Impact factor: 29.690

2.  Cardiovascular system in Marfan's syndrome and in idiopathic dilatation of the ascending aorta.

Authors:  C A WAGENVOORT; H N NEUFELD; J E EDWARDS
Journal:  Am J Cardiol       Date:  1962-04       Impact factor: 2.778

3.  The marfan's syndrome. In vitro study of collagen metabolism in tissue specimens of the aorta.

Authors:  T Krieg; P K Müller
Journal:  Exp Cell Biol       Date:  1977

Review 4.  The Marfan syndrome: diagnosis and management.

Authors:  R E Pyeritz; V A McKusick
Journal:  N Engl J Med       Date:  1979-04-05       Impact factor: 91.245

Review 5.  [Cardiovascular manifestations of Marfan's syndrome (author's transl)].

Authors:  I Kühl; G Fricke
Journal:  Klin Wochenschr       Date:  1973-12-01

6.  Letter: Collagen of Marfan syndrome is abnormally soluble.

Authors:  R E Priest; J F Moinuddin; J H Priest
Journal:  Nature       Date:  1973-10-05       Impact factor: 49.962

7.  Parental age effects on the occurrence of new mutations for the Marfan syndrome.

Authors:  J L Murdoch; B A Walker; V A McKusick
Journal:  Ann Hum Genet       Date:  1972-03       Impact factor: 1.670

8.  Collagen metabolism of the skin in Marfan's syndrome.

Authors:  O Laitinen; J Uitto; M Iivanainen; M Hannuksela; K I Kivirikko
Journal:  Clin Chim Acta       Date:  1968-09       Impact factor: 3.786

9.  The Marfan syndrome and cardiac surgery.

Authors:  Z Davis; J R Pluth; E R Giuliani
Journal:  J Thorac Cardiovasc Surg       Date:  1978-04       Impact factor: 5.209

10.  Composite replacement of the aortic valve and ascending aorta.

Authors:  J E Mayer; W G Lindsay; Y Wang; C R Jorgensen; D M Nicoloff
Journal:  J Thorac Cardiovasc Surg       Date:  1978-12       Impact factor: 5.209

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  3 in total

1.  Marfan syndrome: absence of type I or III collagen structural defects in 25 patients.

Authors:  V R Harley; D Chan; J G Rogers; W G Cole
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Homozygosity for autosomal dominant Marfan syndrome.

Authors:  J Chemke; R Nisani; A Feigl; R Garty; M Cooper; Y Bårash; D Duksin
Journal:  J Med Genet       Date:  1984-06       Impact factor: 6.318

3.  [Marfan syndrome. A contribution to forensic medicine cases].

Authors:  R Vock; E Schulz
Journal:  Z Rechtsmed       Date:  1986
  3 in total

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