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Rapidly progressive mitral valve stenosis in patients with acromelic dysplasia

Published online by Cambridge University Press:  12 January 2017

Gabriel Rama
Affiliation:
New York Presbyterian – Morgan Stanley Children’s Hospital of New York, Columbia University Medical Center, Division of Pediatric Cardiology, New York, New York, United States of America
Wendy K. Chung
Affiliation:
Division of Molecular Genetics, New York, New York, United States of America
Christopher M. Cunniff
Affiliation:
New York Presbyterian – Phyllis and David Komansky Center for Children’s Health, Weill Cornell Medical Center, Division of Clinical Genetics, New York, New York, United States of America
Usha Krishnan*
Affiliation:
New York Presbyterian – Morgan Stanley Children’s Hospital of New York, Columbia University Medical Center, Division of Pediatric Cardiology, New York, New York, United States of America
*
Correspondence to: U. Krishnan, MD, Associate Professor, Division of Pediatric Cardiology, Columbia University Medical Center, 3959 Broadway, New York, NY 10032, United States of America. Tel: (212) 305 4436; Fax: (212) 342-1443; E-mail: [email protected]

Abstract

Acromelic dysplasias are a group of skeletal dysplasias characterised by short-limbed short stature with other distinctive phenotypic features including small hands and feet and stiff joints. Geleophysic dysplasia is an acromelic dysplasia that is associated with characteristic facial features, progressive cardiac valvular thickening, and tracheal stenosis. Owing to overlapping clinical features with other types of short-limbed skeletal dysplasias, it is important to make a precise diagnosis as they have different cardiac morbidity and mortality. We present the cases of three patients with geleophysic dysplasia and progressive mitral valve disease to emphasise the natural history of this disorder and provide guidance regarding cardiac health supervision in these individuals.

Type
Brief Report
Copyright
© Cambridge University Press 2017 

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