Searchable abstracts of presentations at key conferences in endocrinology

ea0017oc2 | Endocrinology 1 | BSPED2008

Persistent AVP production and hyponatraemia in a male infant with an activating mutation of the AVPR2 and his heterozygous mother: new insights into NSAID

Gupta S , Cheetham T , Lambert H , Roberts C , Bourn D , Coulthard M , Ball S

Introduction: The Nephrogenic syndrome of inappropriate antidiuresis (NSIAD) is an X-linked condition characterised by reduced renal water clearance and hyponatraemia resulting from gain of function mutations in the type 2 Vasopressin (AVP) receptor (AVPR2). Female carriers were thought not to express a phenotype. We describe a kindred with NSIAD, highlighting molecular and physiological characteristics that extend understanding of this condition and of AVP production.<p c...