Document Detail

ELN gene triplication responsible for familial supravalvular aortic aneurysm.
MedLine Citation:
PMID:  24932728     Owner:  NLM     Status:  Publisher    
Supravalvular aortic aneurysms are less frequent than abdominal ones. Among Supravalvular aortic aneurysm aetiologies, we focused on dystrophic lesions as they can be secondary to genetic causes such as elastin anomaly. We report on a familial 7q11.23 triplication - including the ELN gene - segregating with a supravalvular aortic aneurysm. During her first pregnancy, our index patient was diagnosed with tuberous sclerosis and with a Supravalvular aortic aneurysm. The foetus was affected equally. For the second pregnancy, parents applied for preimplantation diagnosis, and a subsequent prenatal diagnosis was offered to the couple, comprising TSC1 molecular analysis, karyotype, and multiplex ligation probe amplification. TSC1 mutation was not found on foetal deoxyribo nucleic acid. Foetal karyotype was normal, but multiplex ligation probe amplification detected a 7q11.23 duplication. Quantitative-polymerase chain reaction and array-comparative genomic hybridisation carried out to further assess this chromosome imbalance subsequently identified a 7q11.23 triplication involving ELN and LIMK1. Foetal heart ultrasound identified a Supravalvular aortic aneurysm. A familial screening was offered for the 7q11.23 triplication and, when found, heart ultrasound was performed. The triplication was diagnosed in our index case as well as in her first child. Of the 17 individuals from this family, 11 have the triplication. Of the 11 individuals with the triplication, 10 were identified to have a supravalvular aortic aneurysm. Of them, two individuals received a medical treatment and one individual needed surgery. We provide evidence of supravalvular aortic aneurysm segregating with 7q11.23 triplication in this family. We would therefore recommend cardiac surveillance for individuals with 7q11.23 triplication. It would also be interesting to offer a quantitative-polymerase chain reaction or an array-comparative genomic hybridisation to a larger cohort of patients presenting with isolated supravalvular aortic aneurysm, as it may provide further information.
Anne-Sophie Guemann; Joris Andrieux; Florence Petit; Emmanuel Halimi; Sonia Bouquillon; Sylvie Manouvrier-Hanu; Jiddeke Van De Kamp; Catherine Boileau; Nadine Hanna; Guillaume Jondeau; Guy Vaksmann; Veronique Houfflin-Debarge; Muriel Holder-Espinasse
Related Documents :
24107698 - Anesthetic and hemodynamic management of a rare case of brucella multivalvular endocard...
23895668 - Two- and three-dimensional transthoracic echocardiography in the assessment of acquired...
24995068 - Combined total arch replacement and bypass from the ascending aorta to the bilateral pr...
24778138 - Balloon remodeling of complex anterior communicating artery aneurysms: technical consid...
17826248 - The rare case of a symptomatic atherosclerotic aneurysm of the superior epigastric arte...
25170238 - Nonselective β-blockers may induce development of portal vein thrombosis in cirrhosis.
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2014-6-16
Journal Detail:
Title:  Cardiology in the young     Volume:  -     ISSN:  1467-1107     ISO Abbreviation:  Cardiol Young     Publication Date:  2014 Jun 
Date Detail:
Created Date:  2014-6-16     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  9200019     Medline TA:  Cardiol Young     Country:  -    
Other Details:
Languages:  ENG     Pagination:  1-6     Citation Subset:  -    
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine

Previous Document:  Hydrographic processes driven by seasonal monsoon system affect siphonophore assemblages in tropical...
Next Document:  Genetic and Ecological Outcomes of Inga vera Subsp. affinis (Leguminosae) Tree Plantations in a Frag...