BMC pediatrics · 2025
Sagittal craniosynostosis with Moebius syndrome; case illustration: first case in the literatüre.
СтатьяКлинический случайОбзорНазвание и аннотация: Перевод в очереди
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.
Kuzucu Pelin, Kale Aydemir, Asadov İmran, Börcek Alp Özgün
Аннотация
BACKGROUND: Our aim in this article is to contribute to the clinical findings of Moebius syndrome with the association of synostosis published for the first time.
CASE PRESENTATION: In 2023, the Pediatric Neurosurgery Department operated sagittal synostosis case with Moebius syndrome was retrieved from the neurosurgery archive with literatüre review. A 6-month-old girl who could not close her eyes and mouth after birth was followed up in another hospital with the diagnosis of Moebius Syndrome and was referred to us because of cranial deformity.
CONCLUSION: Moebius syndrome is a syndrome whose cause and clinical framework still need to be fully clarified and is being updated with studies. For this reason, it is essential to recognize the clinical findings seen in patients well, to direct them to genetic research if necessary, and to pay attention to new manifestations that may be added in this context in terms of scientific transfer.
CASE PRESENTATION: In 2023, the Pediatric Neurosurgery Department operated sagittal synostosis case with Moebius syndrome was retrieved from the neurosurgery archive with literatüre review. A 6-month-old girl who could not close her eyes and mouth after birth was followed up in another hospital with the diagnosis of Moebius Syndrome and was referred to us because of cranial deformity.
CONCLUSION: Moebius syndrome is a syndrome whose cause and clinical framework still need to be fully clarified and is being updated with studies. For this reason, it is essential to recognize the clinical findings seen in patients well, to direct them to genetic research if necessary, and to pay attention to new manifestations that may be added in this context in terms of scientific transfer.