Male infant with Noonan syndrome with


Journal

BMJ case reports
ISSN: 1757-790X
Titre abrégé: BMJ Case Rep
Pays: England
ID NLM: 101526291

Informations de publication

Date de publication:
28 Sep 2022
Historique:
entrez: 28 9 2022
pubmed: 29 9 2022
medline: 1 10 2022
Statut: epublish

Résumé

Noonan syndrome (NS) is a congenital disease with characteristic facial features as well as heart disease, short stature and thoracic abnormalities. More than eighty per cent of patients with NS show several cardiac disorders including pulmonary valvular stenosis, hypertrophic cardiomyopathy (HCM) and/or atrial septal defects. HCM is a serious cardiac comorbidity in patients with NS, especially in those who are diagnosed within 6 months of age with congestive heart failure. Arrhythmia with or without HCM in NS is a rare comorbidity with a complicated clinical course and poor prognosis.In this manuscript, we present the case of a male infant with NS with

Identifiants

pubmed: 36171012
pii: 15/9/e250342
doi: 10.1136/bcr-2022-250342
pmc: PMC9528629
pii:
doi:

Substances chimiques

Flecainide K94FTS1806
Amiodarone N3RQ532IUT

Types de publication

Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© BMJ Publishing Group Limited 2022. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Références

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Auteurs

Mao Hagino (M)

Department of Paediatrics, Tohoku University Hospital, Sendai, Japan.

Chiharu Ota (C)

Department of Paediatrics, Tohoku University Hospital, Sendai, Japan chiharu.ota.e8@tohoku.ac.jp.

Takehiko Onoki (T)

Department of Paediatrics, Tohoku University Hospital, Sendai, Japan.

Shinya Iwasawa (S)

Department of Paediatrics, Tohoku University Hospital, Sendai, Japan.

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Classifications MeSH