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Published in 2023 at "Journal of genetic counseling"
DOI: 10.1002/jgc4.1706
Abstract: Families of children with developmental delays but no diagnosed genetic condition may benefit from connection to genetic systems of care. This work examines the role of occupational therapy as a space for families of pediatric…
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Keywords:
patients genetic;
occupational therapists;
referral networks;
networks pediatric ... See more keywords
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Published in 2019 at "Neuroepidemiology"
DOI: 10.1159/000501102
Abstract: Background: Genetic myopathy is a clinically and genetically heterogeneous group of genetic disorders characterized by progressive degeneration of skeletal muscles. Epidemiological studies of genetic myopathy have not yet been performed in Korea. Objectives: This study…
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Keywords:
patients genetic;
prevalence;
genetic myopathy;
socioeconomic status ... See more keywords
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Published in 2023 at "Journal of Child Neurology"
DOI: 10.1177/08830738221147805
Abstract: Neonatal hypoxic-ischemic encephalopathy is a clinical phenomenon that often results from perinatal asphyxia. To mitigate secondary neurologic injury, prompt initial assessment and diagnosis is needed to identify patients eligible for therapeutic hypothermia. However, occasionally neonates…
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Keywords:
patients genetic;
hypoxic ischemic;
genetic susceptibility;
ischemic encephalopathy ... See more keywords
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Published in 2022 at "Healthcare"
DOI: 10.3390/healthcare10030485
Abstract: This case report presents the treatment of a 33-year-old patient with a genetic, generalized microdontia of permanent teeth. Microdontia is a developmental dental anomaly of the teeth characterized by a decrease in their size. In…
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Keywords:
patients genetic;
aesthetic functional;
microdontia;
rehabilitation patients ... See more keywords