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Secondary Hirata Syndrome in a Neonate: Practical Approach and Management

Alessandro Perri1, Simona Fattore1, Annamaria Sbordone1

  • 1Department of Woman and Child Health Sciences, Child Health Area, University Hospital Agostino Gemelli, Fondazione Policlinico Universitario A. Gemelli IRCCS, 00168 Rome, Lazio, Italy.

JCEM Case Reports
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PubMed

Keywords:
Hiratainsulin antibodiesinsulin autoimmune syndromeneonatal hypoglycemianeonate

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Hypertrophic cardiomyopathy, or HCM, is an autosomal dominant genetic disorder characterized by asymmetric left ventricular hypertrophy without ventricular dilation. It is more common in men and is typically diagnosed in young, athletic adults.EtiologyHCM is primarily genetic and is caused by mutations in genes encoding sarcomeric proteins. Researchers have identified over 1400 mutations across at least 11 different genes. Among these, the most frequently occurring mutations are found in the...
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