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Barth Syndrome with Late-Onset Cardiomyopathy: A Missed Opportunity for Diagnosis
Leanne Woiewodski1, David Ezon2, James Cooper2
1Geisinger Commonwealth School of Medicine, Scranton, PA.
Insights
Barth syndrome, a rare genetic condition, can present with neutropenia and growth delay. Early recognition of these signs is crucial for timely diagnosis and management, even with late-onset heart failure.
Area of Science:
- Pediatric genetics
- Cardiology
- Rare diseases
Background:
- Barth syndrome is a rare X-linked genetic disorder.
- Key features include neutropenia, growth delay, and cardiomyopathy.
- Diagnosis can be challenging, often leading to delayed identification.
Abstract:
A male infant presented with neutropenia, growth delay, and death of a maternal uncle at age 2 years. Despite extensive evaluation over 10 years, Barth syndrome was not diagnosed until he presented in acute heart failure. Although late-onset cardiomyopathy is rare, persistence of common Barth features should have enabled earlier diagnosis.
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