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Balloon angioplasty for bilateral severe peripheral pulmonary artery stenoses associated with chondrodysplasia punctata: a case report

Published online by Cambridge University Press:  21 November 2024

Kiyotaka Go Open the ORCID record for Kiyotaka Go [Opens in a new window] ,
Kazushi Yasuda  and
Taichi Kato Open the ORCID record for Taichi Kato [Opens in a new window]
Kiyotaka Go
Affiliation:
Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan
Kazushi Yasuda
Affiliation:
Department of Cardiology, Aichi Children’s Health and Medical Center, Aichi, Japan
Taichi Kato*
Affiliation:
Department of Pediatrics, Nagoya University Graduate School of Medicine, Nagoya, Japan
*
Corresponding author: Taichi Kato; Email: [email protected]
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Abstract

We present a 2-month-old girl with chondrodysplasia punctata in whom bilateral peripheral pulmonary artery stenoses were successfully treated by transcatheter balloon angioplasty. The minimal diameters of the right and left pulmonary arteries of 1.3 mm and 1.1 mm, respectively, which were dilated using a 4-mm balloon catheter. Balloon angioplasty is feasible and effective for relieving peripheral pulmonary artery stenosis in patients with chondrodysplasia punctata.

Keywords

Chondrodysplasia punctataperipheral pulmonary artery stenosisballoon angioplasty
Type
Brief Report
Information
Cardiology in the Young , First View , pp. 1 - 4
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Copyright
© The Author(s), 2024. Published by Cambridge University Press

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