A unique case of a child with two inherited salt-losing conditions

A Unique Case of a Child with Two Inherited Salt-Losing Conditions DS Gurudutt1, H McCabe2, C O’Brien2, DSF Matthews1 1 Dept of Paediatric Endocrinology, 2 Dept of Paediatric Respiratory Medicine Introduc*on Salt losing conditions can be challenging to manage well during infancy and childhood. Prolonged sodium depletion is known to be associated with growth failure and other problems in young animals1. We describe a unique case of a child with both Salt-Wasting 21-Hydroxylase Deficiency (SW21OHD) and Cystic Fibrosis (CF).