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Singleton Merten Syndrome: A Rare Cause of Early Onset Aortic Stenosis
Joint Authors
Mungee, Sudhir
Ghadiam, Harshavardhan
Source
Issue
Vol. 2017, Issue 2017 (31 Dec. 2017), pp.1-3, 3 p.
Publisher
Hindawi Publishing Corporation
Publication Date
2017-02-21
Country of Publication
Egypt
No. of Pages
3
Main Subjects
Abstract EN
Singleton Merten syndrome (SMS) is a rare autosomal dominant genetic disorder with variable expression.
Its characteristic features include abnormal aortic calcification, abnormal ossification of extremities, and dental anomalies.
We present a young man with dyspnea who was noted to have aortic stenosis in the background of glaucoma, psoriasis, dental anomalies, hand and foot deformities, Achilles tendinitis, osteopenia, and nephrolithiasis.
The conglomeration of features led to the diagnosis of SMS.
His mother had a very similar phenotype.
American Psychological Association (APA)
Ghadiam, Harshavardhan& Mungee, Sudhir. 2017. Singleton Merten Syndrome: A Rare Cause of Early Onset Aortic Stenosis. Case Reports in Cardiology،Vol. 2017, no. 2017, pp.1-3.
https://search.emarefa.net/detail/BIM-1144198
Modern Language Association (MLA)
Ghadiam, Harshavardhan& Mungee, Sudhir. Singleton Merten Syndrome: A Rare Cause of Early Onset Aortic Stenosis. Case Reports in Cardiology No. 2017 (2017), pp.1-3.
https://search.emarefa.net/detail/BIM-1144198
American Medical Association (AMA)
Ghadiam, Harshavardhan& Mungee, Sudhir. Singleton Merten Syndrome: A Rare Cause of Early Onset Aortic Stenosis. Case Reports in Cardiology. 2017. Vol. 2017, no. 2017, pp.1-3.
https://search.emarefa.net/detail/BIM-1144198
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references
Record ID
BIM-1144198