Congenital nephrogenic diabetes insipidus presenting as osmotic demyelination syndrome in infancy
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DOI: 10.1097/md.0000000000028552
Abstract: Abstract Rationale: Almost 90% of congenital nephrogenic diabetes insipidus (NDI) cases are caused by mutations in the arginine vasopressin receptor 2 gene, which has X-linked recessive inheritance. Although NDI is commonly diagnosed in early infancy… read more here.
Keywords: osmotic demyelination; congenital nephrogenic; nephrogenic diabetes; diagnosis ... See more keywords