MedElevator Войти в исследования
← Поиск публикаций

DOI 10.1016/j.mjafi.2022.09.004

Медицинская библиотека · Medical journal, Armed Forces India · 2022

Ophthalmologic manifestations of organoid nevus syndrome: A series of 13 cases.

Singh Pallavi, Bajaj Mandeep S, Agrawal Sahil, Kaginalkar Ananya, Das Deepsekhar

СтатьяПеревод в очереди

Аннотация

BACKGROUND

The organoid nevus syndrome is a rare neurocutaneous syndrome typified by cutaneous sebaceous nevus, seizures and epibulbar choristomas. The condition is associated with multiple ocular abnormalities. Herein, the authors aim to study and report the ophthalmic features of cases diagnosed with organoid nevus syndrome.

METHODS

The authors retrospectively evaluated the records of patients with the organoid nevus syndrome who had presented to a tertiary care eye hospital in northern India. The ocular features were studied and entered in MS excel and the data were evaluated.

RESULTS

Data of 13 patients with the organoid nevus syndrome were found. All 13 patients had cutaneous features in the form of Sebaceous nevus of Jadasson, 8 patients had alopecia of the scalp area, 2 had history seizures and 10 had arachnoid cysts on neuroimaging of the head. All 13 patients had a complex choristoma involving the ocular surface.

CONCLUSIONS

We conclude that the most common ophthalmologic features associated with organoid nevus are complex choristoma of the bulbar surface, scleral coat calcification and upper eyelid coloboma.

Для цитирования: Singh Pallavi, Bajaj Mandeep S, Agrawal Sahil, Kaginalkar Ananya, Das Deepsekhar. Ophthalmologic manifestations of organoid nevus syndrome: A series of 13 cases.. Medical journal, Armed Forces India. 2022. DOI: 10.1016/j.mjafi.2022.09.004.
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.