Evaluation of neonatal hypotonia [Hipotonik yenido?anin de?erlendirilmesi]

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dc.contributor.authorAydin K.
dc.date.accessioned2020-03-26T17:18:54Z
dc.date.available2020-03-26T17:18:54Z
dc.date.issued2007
dc.departmentSelçuk Üniversitesien_US
dc.description.abstractHypotonia is one of the most important neurologic findings in neonatal period. The condition is usually evident at birth or is identified during early life as poor muscle tone results in an inability to maintain normal posture during movement and rest. Although neonatal hypotonia is frequently and easily recognized by the first pediatric examination of the newborn, the diagnostic work up is often complex and difficult. Advances in genetics and neurosciences have lead to recognition of newer diagnostic entities, and rapid molecular diagnosis is now possible for several conditions such as spinal muscular atrophy, congenital muscular dystrophies, and congenital myopathies. Mainly, causes of hypotonia can be divided as central or peripheral. Central causes are hypoxic lesions of the brain, chromosomal abnormalities, brain malformations, and metabolic disorders. Peripheral causes are spinal muscular atrophy and muscle disorders. Neurologic examination, neuroimaging, karyotype analysis, and molecular genetic tests are the most helpful diagnostic tools.en_US
dc.identifier.endpage142en_US
dc.identifier.issn1016-5134en_US
dc.identifier.issue11en_US
dc.identifier.scopusqualityN/Aen_US
dc.identifier.startpage139en_US
dc.identifier.urihttps://hdl.handle.net/20.500.12395/21762
dc.identifier.volume19en_US
dc.indekslendigikaynakScopusen_US
dc.language.isotren_US
dc.relation.ispartofSENDROMen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.selcuk20240510_oaigen_US
dc.titleEvaluation of neonatal hypotonia [Hipotonik yenido?anin de?erlendirilmesi]en_US
dc.typeReviewen_US

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