Literature DB >> 6856406

Cardiovascular manifestations in the Larsen syndrome.

E A Kiel, J L Frias, B E Victorica.   

Abstract

The Larsen syndrome consists of a skeletal dysplasia with multiple joint dislocations and a characteristic facies. The basis of the abnormalities is felt to be a generalized mesenchymal disorder involving connective tissues. More than 80 cases have been reported in the literature with isolated reports of congenital cardiac septal defects and acquired abnormalities of the aorta and mitral valve. A case with marked aortic dilation and insufficiency as well as an aneurysm of the ductus arteriosus is presented. The aortic lesions are similar to those described in other connective tissue disorders, particularly the Marfan syndrome. Previous reports of ductal aneurysms have not revealed an association with connective tissue disorders, but have described a significant morbidity. In summary, patients with the Larsen syndrome are likely to have cardiac lesions similar to those classically associated with the Marfan syndrome; these patients deserve a careful investigation for cardiac anomalies. These aortic lesions may be as prognostically significant as cardiac lesions in the Marfan syndrome.

Entities:  

Mesh:

Year:  1983        PMID: 6856406

Source DB:  PubMed          Journal:  Pediatrics        ISSN: 0031-4005            Impact factor:   7.124


  9 in total

1.  Larsen syndrome--lethal variety.

Authors:  M L Kulkarni; Zaheeruddin Mohammed; Preethi M Kulkarni
Journal:  Indian J Pediatr       Date:  2005-12       Impact factor: 1.967

2.  Pneumoperitoneum in a patient with Larsen syndrome.

Authors:  Satoki Inoue; Yasumitsu Nomura; Masahiko Kawaguchi
Journal:  J Anesth       Date:  2013-11-09       Impact factor: 2.078

3.  A molecular and clinical study of Larsen syndrome caused by mutations in FLNB.

Authors:  Louise S Bicknell; Claire Farrington-Rock; Yousef Shafeghati; Patrick Rump; Yasemin Alanay; Yves Alembik; Navid Al-Madani; Helen Firth; Mohammad Hassan Karimi-Nejad; Chong Ae Kim; Kathryn Leask; Melissa Maisenbacher; Ellen Moran; John G Pappas; Paolo Prontera; Thomy de Ravel; Jean-Pierre Fryns; Elizabeth Sweeney; Alan Fryer; Sheila Unger; L C Wilson; Ralph S Lachman; David L Rimoin; Daniel H Cohn; Deborah Krakow; Stephen P Robertson
Journal:  J Med Genet       Date:  2006-06-26       Impact factor: 6.318

4.  Aneurysm of the ductus arteriosus in a patient with Larsen syndrome.

Authors:  Bo-Kyung Je; So-Young Yoo; Whal Lee; Woo Sun Kim; In-One Kim
Journal:  Pediatr Radiol       Date:  2006-09-28

5.  Importance of the clinical recognition of Loeys-Dietz syndrome in the neonatal period.

Authors:  Anji T Yetman; Rebecca S Beroukhim; Dunbar D Ivy; David Manchester
Journal:  Pediatrics       Date:  2007-05       Impact factor: 7.124

Review 6.  Aneurysm of the ductus arteriosus in the neonate: three case reports with a review of the literature.

Authors:  J T Lund; D Hansen; V Brocks; M B Jensen; J R Jacobsen
Journal:  Pediatr Cardiol       Date:  1992-10       Impact factor: 1.655

7.  Localization of a gene for autosomal dominant Larsen syndrome to chromosome region 3p21.1-14.1 in the proximity of, but distinct from, the COL7A1 locus.

Authors:  M Vujic; K Hallstensson; J Wahlström; A Lundberg; C Langmaack; T Martinson
Journal:  Am J Hum Genet       Date:  1995-11       Impact factor: 11.025

8.  Clinical diagnosis of Larsen syndrome, Stickler syndrome and Loeys-Dietz syndrome in a 19-year old male: a case report.

Authors:  N Riise; B R Lindberg; M A Kulseth; S O Fredwall; R Lundby; M-E Estensen; L Drolsum; E Merckoll; K Krohg-Sørensen; B Paus
Journal:  BMC Med Genet       Date:  2018-08-31       Impact factor: 2.103

Review 9.  Guidelines for genetic skeletal dysplasias for pediatricians.

Authors:  Sung Yoon Cho; Dong-Kyu Jin
Journal:  Ann Pediatr Endocrinol Metab       Date:  2015-12-31
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.