The Indian Journal of Pediatrics

, Volume 86, Issue 3, pp 296–298 | Cite as

Alström Syndrome Presenting as Isolated Dilated Cardiomyopathy

  • Gayatri Nerakh
  • Prajnya RanganathEmail author
Clinical Brief


Cardiomyopathy is an etiologically heterogeneous condition, and non-syndromic as well as syndromic genetic causes are identified in a significant proportion of cases without a known acquired cause. The present report describes a 2-mo-old boy who presented initially with a referral diagnosis of isolated dilated cardiomyopathy, without any associated dysmorphism or malformations, and with history of similar cardiac disease and early infantile death in an elder male sibling. Next generation sequencing (NGS) based multigene panel testing of the cardiomyopathy-associated genes was done which revealed the diagnosis of Alström syndrome, based on which appropriate management and surveillance could be planned for the child and accurate genetic counseling could be provided to the parents. This report reiterates the fact that genetic testing for cardiomyopathy without an obvious acquired cause helps in identification of the underlying etiology, appropriate management, early diagnosis of syndromic forms, and monitoring and pre-symptomatic intervention for associated extracardiac complications.


Dilated cardiomyopathy Alström syndrome ALMS1 gene 



The authors wish to thank the patient and his family for their cooperation.

Author Contributions

GN: Clinical evaluation and diagnosis of patient, review of literature, and preparation of manuscript; PR: Clinical evaluation, diagnosis and management of patient, review of literature, preparation of manuscript. PR will act as guarantor for this paper.

Compliance with Ethical Standards

Conflict of Interest


Source of Funding


Ethical Approval

Written informed consent obtained from the father of the child for publication of clinical photographs and case details.


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Copyright information

© Dr. K C Chaudhuri Foundation 2018

Authors and Affiliations

  1. 1.Department of Medical GeneticsNizam’s Institute of Medical SciencesHyderabadIndia
  2. 2.Diagnostics Division, Centre for DNA Fingerprinting and DiagnosticsHyderabadIndia

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