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Cardiovascular manifestations of Hutchinson–Gilford progeria syndrome

Part of: Echocardiography

Published online by Cambridge University Press:  13 January 2022

Andreia Palma Open the ORCID record for Andreia Palma [Opens in a new window] ,
Patrícia V. Silva  and
António Pires
Andreia Palma*
Affiliation:
Department of Paediatric Cardiology, Referral Centre for Congenital Cardiac Defects, CHUC, Portugal, Coimbra, Portugal
Patrícia V. Silva
Affiliation:
Department of Paediatric Cardiology, Referral Centre for Congenital Cardiac Defects, CHUC, Portugal, Coimbra, Portugal
António Pires
Affiliation:
Department of Paediatric Cardiology, Referral Centre for Congenital Cardiac Defects, CHUC, Portugal, Coimbra, Portugal
*
Author for correspondence: Andreia Palma, Hospital Pediátrico de Coimbra, Avenida Dr. Afonso Romão, 3000-602 Coimbra, Portugal. Tel:+351965067190/ +351239488700. E-mail: andreia.fmp91@gmail.com
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Abstract

Cardiovascular complications are the most frequent cause of death in patients with the Hutchinson–Gilford progeria syndrome. However, due to its rarity, studying the course of cardiac abnormalities has been a challenge. The cardiovascular phenotype helps to provide greater insight into the natural history of these abnormalities.

Type
Brief Report
Information
Cardiology in the Young , Volume 32 , Issue 9 , September 2022 , pp. 1533 - 1535
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Copyright
© The Author(s), 2022. Published by Cambridge University Press

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References

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