Abstract
A 4-month-old boy was presented with failure to thrive, refusal to feed, delayed motor development, truncal hypotonia, and head lag. His plasma osmolality and sodium were significantly high, while his urine osmolality was inappropriately low and did not increase after desmopressin administration. Despite his hyperosmolality, he presented with a lack of thirst and became clearly polyuric and polydipsic only at the age of 2 years. Initial treatment with indomethacin was ineffective, while the combination of hydrochlorothiazide and amiloride was effective and well tolerated. © 2006 Society of the European Journal of Endocrinology.
Cite
CITATION STYLE
Marcovecchio, M. L. (2006). An infant with chronic hypernatremia. In European Journal of Endocrinology, Supplement (Vol. 155). https://doi.org/10.1530/eje.1.02269
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