Indian pediatrics · 2015
Multiple Pituitary Hormone Deficiency, Empty Sella and Ectopic Neurohypophysis in Turner Syndrome.
Клинический случайСтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Dutta Deep, Selvan Chitra, Mukhopadhyay Satinath
Аннотация
BACKGROUND: Multiple pituitary hormone deficiency and Turner syndrome have overlapping features in peripubertal girls and is a diagnostic challenge.
CASE CHARACTERISTICS: 16-year-old girl having Turner phenotype undergoing evaluation for severe short stature and pubertal arrest.
OBSERVATION: 45,X karyotype, and multiple pituitary hormone deficiency with empty sella.
INTERVENTION: Levothyroxine, growth hormone and ethinyl-estradiol replacement resulted in 11 cm height gain with attainment of puberty over 2 years.
MESSAGE: Patients of Turner syndrome with height <3rd percentile (Turner specific charts) warrant additional pathology evaluation.
CASE CHARACTERISTICS: 16-year-old girl having Turner phenotype undergoing evaluation for severe short stature and pubertal arrest.
OBSERVATION: 45,X karyotype, and multiple pituitary hormone deficiency with empty sella.
INTERVENTION: Levothyroxine, growth hormone and ethinyl-estradiol replacement resulted in 11 cm height gain with attainment of puberty over 2 years.
MESSAGE: Patients of Turner syndrome with height <3rd percentile (Turner specific charts) warrant additional pathology evaluation.