ea0027oc2.3 | Oral Communications 2 (Quick Fire) | BSPED2011
Hughes Claire
, Guasti Leonardo
, Meimaridou Eirini
, Chaung Chen-Hua
, Schimenti John
, King Peter
, Costigan Colm
, Clark Adrian
, Metherell Louise
Introduction: A unique variant of familial glucocorticoid deficiency (FGD) exists in the Irish travelling community, a genetically isolated population with high levels of consanguinity. Affected children develop hypocortisolaemia and raised ACTH but retain normal renin and aldosterone levels. Children also have short stature, evidence of increased chromosomal breakage and natural killer cell deficiency.Methods: We sought areas of homozygosity common to a...