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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| Main Authors: | , , , |
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| Format: | Book |
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Frontiers Media S.A.,
2018-10-01T00:00:00Z.
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| Call Number: |
A1234.567 |
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| Copy 1 | Available |