Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management
المؤلفون المشاركون
Perdicchi, Andrea
Abdolrahimzadeh, Solmaz
Recupero, Santi Maria
Fameli, Valeria
Mollo, Roberto
Contestabile, Maria Teresa
المصدر
العدد
المجلد 2015، العدد 2015 (31 ديسمبر/كانون الأول 2015)، ص ص. 1-11، 11ص.
الناشر
Hindawi Publishing Corporation
تاريخ النشر
2015-09-16
دولة النشر
مصر
عدد الصفحات
11
التخصصات الرئيسية
الملخص EN
Noteworthy heterogeneity exists in the rare diseases associated with childhood glaucoma.
Primary congenital glaucoma is mostly sporadic; however, 10% to 40% of cases are familial.
CYP1B1 gene mutations seem to account for 87% of familial cases and 27% of sporadic cases.
Childhood glaucoma is classified in primary and secondary congenital glaucoma, further divided as glaucoma arising in dysgenesis associated with neural crest anomalies, phakomatoses, metabolic disorders, mitotic diseases, congenital disorders, and acquired conditions.
Neural crest alterations lead to the wide spectrum of iridocorneal trabeculodysgenesis.
Systemic diseases associated with childhood glaucoma include the heterogenous group of phakomatoses where glaucoma is frequently encountered in the Sturge-Weber syndrome and its variants, in phakomatosis pigmentovascularis associated with oculodermal melanocytosis, and more rarely in neurofibromatosis type 1.
Childhood glaucoma is also described in systemic disorders of mitotic and metabolic activity.
Acquired secondary glaucoma has been associated with uveitis, trauma, drugs, and neoplastic diseases.
A database research revealed reports of childhood glaucoma in rare diseases, which do not include glaucoma in their manifestation.
These are otopalatodigital syndrome, complete androgen insensitivity, pseudotrisomy 13, Brachmann-de Lange syndrome, acrofrontofacionasal dysostosis, caudal regression syndrome, and Wolf-Hirschhorn syndrome.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Abdolrahimzadeh, Solmaz& Fameli, Valeria& Mollo, Roberto& Contestabile, Maria Teresa& Perdicchi, Andrea& Recupero, Santi Maria. 2015. Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management. BioMed Research International،Vol. 2015, no. 2015, pp.1-11.
https://search.emarefa.net/detail/BIM-1056700
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Abdolrahimzadeh, Solmaz…[et al.]. Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management. BioMed Research International No. 2015 (2015), pp.1-11.
https://search.emarefa.net/detail/BIM-1056700
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Abdolrahimzadeh, Solmaz& Fameli, Valeria& Mollo, Roberto& Contestabile, Maria Teresa& Perdicchi, Andrea& Recupero, Santi Maria. Rare Diseases Leading to Childhood Glaucoma: Epidemiology, Pathophysiogenesis, and Management. BioMed Research International. 2015. Vol. 2015, no. 2015, pp.1-11.
https://search.emarefa.net/detail/BIM-1056700
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references
رقم السجل
BIM-1056700
قاعدة معامل التأثير والاستشهادات المرجعية العربي "ارسيف Arcif"
أضخم قاعدة بيانات عربية للاستشهادات المرجعية للمجلات العلمية المحكمة الصادرة في العالم العربي
تقوم هذه الخدمة بالتحقق من التشابه أو الانتحال في الأبحاث والمقالات العلمية والأطروحات الجامعية والكتب والأبحاث باللغة العربية، وتحديد درجة التشابه أو أصالة الأعمال البحثية وحماية ملكيتها الفكرية. تعرف اكثر