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https://doi.org/10.14300/mnnc.2019.14096

Hystyocytoid cardiomyopathy in the newborn with extremely low body weight

[Notes from practice]
Ludmila Kulida; Olga Saryeva; Mariya Malysheva;

A description of the clinical observation of histiocytoid cardiomyopathy in an extremely low birth weight of a newborn girl is given. This is a genetically determined form of cardiomyopathy associated with a mutation of the gene encoding the proteins of electron mitochondrial transport. Observation reflects the main clinical manifestations and features of myocardial restructuring characteristic of this form of cardiomyopathy.

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Keywords: histiocytoid cardiomyopathy, mitochondrial myopathy, cardiac rhythm disturbance, a newborn with extremely low body weight