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

Gurudutt, Divya; McCabe, Helen; O’Brien, Christopher J.; Matthews, Debbie

doi:10.1530/endoabs.36.p2

EJEA

2014

DOI: 10.1530/endoabs.36.p2

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

Divya Gurudutt¹,

Helen McCabe²,

Christopher J. O’Brien³

et al.

Abstract: 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 animals 1. We describe a unique case of a child with both Salt-Wasting 21-Hydroxylase Deficiency (SW21OHD) and Cystic Fibrosis (CF).

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

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