Highlights the rare association between congenital physiologically corrected transposition and hypertrophic obstructive cardiomyopathy.
Clinicians should consider hypertrophic obstructive cardiomyopathy in corrected transposition; extends sparse case reports but leaves open prevalence and management.
Two cases of congenital physiologically corrected transposition are reported in which there was associated hypertrophic obstructive cardiomyopathy, in one case affecting mainly the left-sided (morphological right) ventricle, and in the other the right-sided (morphological left) ventricle. In the former there was dextrorotation with mesocardia.
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Honey et al. (1971) studied this question.
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