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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Detalles Bibliográficos
Autores principales: Alzarka, Bakri, Usala, Rachel, Whitehead, Matthew T., Ahn, Sun-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
Materias:
Pediatrics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193093/
https://www.ncbi.nlm.nih.gov/pubmed/30364227
http://dx.doi.org/10.3389/fped.2018.00273

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6193093/
https://www.ncbi.nlm.nih.gov/pubmed/30364227
http://dx.doi.org/10.3389/fped.2018.00273

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