Hyponatremia: An Unusual Presentation in a Neonate With Chromosome 1q21.1 Deletion Syndrome

Chromosome 1q21.1 deletion syndrome is associated with a wide variety of clinical features including mild to moderate mental retardation, microcephaly, cardiac abnormalities, and cataracts. We report an unusual case of a premature neonate with persistent hyponatremia, markedly elevated plasma argini...

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Hauptverfasser: Bakri Alzarka (VerfasserIn), Rachel Usala (VerfasserIn), Matthew T. Whitehead (VerfasserIn), Sun-Young Ahn (VerfasserIn)
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Veröffentlicht: Frontiers Media S.A., 2018-10-01T00:00:00Z.
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