Allan–Herndon–Dudley syndrome (clinical case)
AbstractThe article presents a case of clinical observation of a patient with a rare genetic syndrome. The peculiarity of the clinical case is the difficulty of diagnosis in children at an early age. The article shows the role of studying the history, clinical and laboratory parameters and the value of genetic research.
Keywords:genetics, gene mutation, thyroid hormones, children, damage to the nervous system
Endocrinology: News, Opinions, Training. 2018; 7 (4): 58-61. doi: 10.24411/2304-9529-2018-14008.