MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1097/gim.0b013e3181634edf

Медицинская библиотека · Genetics in medicine : official journal of the American College of Medical Genetics · 2008

Parathyroid hormone reserve in 22q11.2 deletion syndrome.

Kapadia Chirag R, Kim Yuran E, McDonald-McGinn Donna M, Zackai Elaine H, Katz Lorraine E Levitt

СтатьяПеревод пока не подготовлен

Аннотация

OBJECTIVE

We hypothesized that most patients with 22q11.2 deletion and a history of hypocalcemia have inadequate parathyroid function, manifested by intact parathyroid hormone levels below normal. We aimed to evaluate intact parathyroid hormone levels both during normocalcemia and at hypocalcemia, in this population.

STUDY

DESIGN

Retrospective chart review of 103 patients with 22q11.2 deletion born since 1997 and cared for at the Children's Hospital of Philadelphia. Calcium and intact parathyroid hormone drawn simultaneously were recorded, along with clinical presentation at hypocalcemia.

RESULTS

Forty-seven simultaneous Ca/intact parathyroid hormone values were available. Seventy-nine percent of calcium levels and 81% of parathyroid hormone levels were within normal range. There were 19 patients with a history of symptomatic hypocalcemia, for whom any available simultaneous Ca/parathyroid hormone levels, before, during, or after hypocalcemia were analyzed. In this subgroup, 59% of calcium and 76% of parathyroid hormone levels were normal. None had an intact parathyroid hormone of >39.2 pg/mL at hypocalcemia. Seventy-three percent of hypocalcemic events had a precipitating stressor.

CONCLUSIONS

Hypoparathyroidism in 22q11.2 deletion is mild, manifesting as a phenomenon of decreased parathyroid hormone reserve. Subjects are normocalcemic most of the time, but are unable to mount elevated intact parathyroid hormone levels, and therefore unable to correct hypocalcemia, in response to stressors.

Для цитирования: Kapadia Chirag R, Kim Yuran E, McDonald-McGinn Donna M, Zackai Elaine H, Katz Lorraine E Levitt. Parathyroid hormone reserve in 22q11.2 deletion syndrome.. Genetics in medicine : official journal of the American College of Medical Genetics. 2008. DOI: 10.1097/gim.0b013e3181634edf.

Предметные рубрики MeSH

Подготовка и перевод публикации
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…

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.

Тип публикации указан по данным источника. Уровень доказательности автоматически не присваивается.