التفاصيل البيبلوغرافية
العنوان: |
A rare case of anophthalmia without any family history and antenatal risk factors |
المؤلفون: |
Kreshnike Dedushi, Fjolla Hyseni, Juna Musa, Kristi Saliaj, Valon Vokshi, Ali Guy, Atiq Bhatti, Abdur Rahman, Muhammad Tahir, Loran Rakovica, Masum Rahman, Jeton Shatri |
المصدر: |
Radiology Case Reports, Vol 16, Iss 12, Pp 3772-3775 (2021) |
بيانات النشر: |
Elsevier, 2021. |
سنة النشر: |
2021 |
المجموعة: |
LCC:Medical physics. Medical radiology. Nuclear medicine |
مصطلحات موضوعية: |
Anophthalmia, Micro-ophthalmia, Magnetic resonance imaging, Teratogens, Medical physics. Medical radiology. Nuclear medicine, R895-920 |
الوصف: |
Anophthalmia is a rare genetic disorder. It is defined as the absence of one or both eyes in a patient. It can be unilateral or bilateral. Based on the absence of anatomical structures, it is divided into primary, secondary, and degenerative anophthalmia. It occurs in an infant with a diabetic mother or any exposure to teratogens. Most of the patients have a positive family history of anophthalmia or related genetic disorder. Its diagnosis is crucial as there is a similar condition called micro ophthalmia. Sometimes it is difficult to differentiate between severe microphthalmia and anophthalmia. We present a case of a 5-day-old infant diagnosed with bilateral anophthalmia. In the majority of the cases of bilateral anophthalmia the patients usually have a positive family history of antenatal exposure to teratogenic substances. But in our case, no family history or antenatal teratogenic exposure was noted. |
نوع الوثيقة: |
article |
وصف الملف: |
electronic resource |
اللغة: |
English |
تدمد: |
1930-0433 |
Relation: |
http://www.sciencedirect.com/science/article/pii/S1930043321006518; https://doaj.org/toc/1930-0433 |
DOI: |
10.1016/j.radcr.2021.09.001 |
URL الوصول: |
https://doaj.org/article/c569e02cc744456d9d31d325b5daa72f |
رقم الانضمام: |
edsdoj.569e02cc744456d9d31d325b5daa72f |
قاعدة البيانات: |
Directory of Open Access Journals |