Literature DB >> 16261269

Severe supravalvar aortic stenosis in familial homozygous hypercholesterolemia.

G Arora1, C D Fraser, D L Kearney, J A Vincent.   

Abstract

Familial homozygous hypercholesterolemia is a rare disease with diverse clinical presentations. Patients often present with cutaneous xanthomas, particularly in the Achilles' tendon. They may have significant cardiovascular involvement, including premature atherosclerotic coronary artery disease and valvar and supravalvar aortic stenosis. Standard therapy includes diet modulation, pharmacotherapy, and lipid apheresis. Rarely, patients require surgical intervention for coronary artery bypass grafting and/or relief of the aortic stenosis. We present the case of a patient with severe progressive supravalvar aortic stenosis that ultimately required surgical resection despite aggressive medical therapy.

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Year:  2006        PMID: 16261269     DOI: 10.1007/s00246-005-5809-0

Source DB:  PubMed          Journal:  Pediatr Cardiol        ISSN: 0172-0643            Impact factor:   1.655


  6 in total

Review 1.  Pharmacologic and surgical treatment of dyslipidemic children and adolescents.

Authors:  J M Hoeg
Journal:  Ann N Y Acad Sci       Date:  1991       Impact factor: 5.691

2.  Characteristic cardiovascular manifestation in homozygous and heterozygous familial hypercholesterolemia.

Authors:  A Kawaguchi; K Miyatake; C Yutani; S Beppu; M Tsushima; T Yamamura; A Yamamoto
Journal:  Am Heart J       Date:  1999-03       Impact factor: 4.749

3.  Extent and severity of atherosclerotic involvement of the aortic valve and root in familial hypercholesterolaemia.

Authors:  L Rallidis; R P Naoumova; G R Thompson; P Nihoyannopoulos
Journal:  Heart       Date:  1998-12       Impact factor: 5.994

Review 4.  A review on the diagnosis, natural history, and treatment of familial hypercholesterolaemia.

Authors:  Dalya Marks; Margaret Thorogood; H Andrew W Neil; Steve E Humphries
Journal:  Atherosclerosis       Date:  2003-05       Impact factor: 5.162

5.  Low-density lipoprotein apheresis as long-term treatment for children with homozygous familial hypercholesterolemia.

Authors:  R J Zwiener; R Uauy; M L Petruska; B A Huet
Journal:  J Pediatr       Date:  1995-05       Impact factor: 4.406

6.  Liver transplantation for homozygous familial hypercholesterolaemia.

Authors:  S P Revell; G Noble-Jamieson; P Johnston; A Rasmussen; N Jamieson; N D Barnes
Journal:  Arch Dis Child       Date:  1995-11       Impact factor: 3.791

  6 in total
  1 in total

1.  Redux valvular surgery with coronary artery bypass graft in familial hypercholesterolemia.

Authors:  Ziadi Jalel; Mleyhi Sobhi; Ben Omrane Skander; Khayati Adel
Journal:  Ann Pediatr Cardiol       Date:  2014-01
  1 in total

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