The Impact of Syndromic Genetic Disorders on Medical Management and Mortality in Pediatric Hypertrophic Cardiomyopathy Patients
Sign Up to like & getrecommendations! Published in 2020 at "Pediatric Cardiology"
DOI: 10.1007/s00246-020-02373-4
Abstract: Hypertrophic cardiomyopathy (HCM) is a prevalent cardiomyopathy in children, with variable etiologies, phenotypes, and associated syndromic genetic disorders (GD). The spectrum of evaluation in this heterogeneous population has not been well described. We aimed to… read more here.
Keywords: syndromic genetic; hypertrophic cardiomyopathy; mortality; genetic disorders ... See more keywords
Peripheral Vestibular Dysfunction Is a Common Occurrence in Children With Non-syndromic and Syndromic Genetic Hearing Loss
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DOI: 10.3389/fneur.2021.714543
Abstract: Hearing loss (HL) is the most common sensory deficit in humans and is frequently accompanied by peripheral vestibular loss (PVL). While often overlooked, PVL is an important sensory dysfunction that may impair development of motor… read more here.
Keywords: hearing loss; syndromic genetic; dysfunction; non syndromic ... See more keywords