hrp0082p3-d1-902 | Pituitary | ESPE2014

A Case of Congenital Isolated ACTH Deficiency due to tbx19 Gene Mutation

Kazachenko Natalya , Tiulpakov Anatoly , Skorodok Yulia , Ivanov Dmitry , Mullakhmetova Zukhra

Objective: To characterise clinical presentation of congenital isolated ACTH deficiency.Methods and results: Clinical and anthropometric data were obtained. Biochemical liver function parameters, blood glucose, insulin, TSH, free thyroxin (FT4), GH, cortisol, and ACTH levels were analyzed. POMC and TBX19 genes were analysed by Sanger sequencing. The girl was born at full-term with normal weight and length. The parents are cousins. At birth cra...