Molecular, Phenotypic Aspects and Therapeutic Horizons of Rare Genetic Bone Disorders
المؤلفون المشاركون
Faruqi, Taha
Dhawan, Naveen
Bahl, Jaya
Gupta, Vineet
Vohra, Shivani
Tu, Khin
Abdelmagid, Samir M.
المصدر
العدد
المجلد 2014، العدد 2014 (31 ديسمبر/كانون الأول 2014)، ص ص. 1-16، 16ص.
الناشر
Hindawi Publishing Corporation
تاريخ النشر
2014-10-22
دولة النشر
مصر
عدد الصفحات
16
التخصصات الرئيسية
الملخص EN
A rare disease afflicts less than 200,000 individuals, according to the National Organization for Rare Diseases (NORD) of the United States.
Over 6,000 rare disorders affect approximately 1 in 10 Americans.
Rare genetic bone disorders remain the major causes of disability in US patients.
These rare bone disorders also represent a therapeutic challenge for clinicians, due to lack of understanding of underlying mechanisms.
This systematic review explored current literature on therapeutic directions for the following rare genetic bone disorders: fibrous dysplasia, Gorham-Stout syndrome, fibrodysplasia ossificans progressiva, melorheostosis, multiple hereditary exostosis, osteogenesis imperfecta, craniometaphyseal dysplasia, achondroplasia, and hypophosphatasia.
The disease mechanisms of Gorham-Stout disease, melorheostosis, and multiple hereditary exostosis are not fully elucidated.
Inhibitors of the ACVR1/ALK2 pathway may serve as possible therapeutic intervention for FOP.
The use of bisphosphonates and IL-6 inhibitors has been explored to be useful in the treatment of fibrous dysplasia, but more research is warranted.
Cell therapy, bisphosphonate polytherapy, and human growth hormone may avert the pathology in osteogenesis imperfecta, but further studies are needed.
There are still no current effective treatments for these bone disorders; however, significant promising advances in therapeutic modalities were developed that will limit patient suffering and treat their skeletal disabilities.
نمط استشهاد جمعية علماء النفس الأمريكية (APA)
Faruqi, Taha& Dhawan, Naveen& Bahl, Jaya& Gupta, Vineet& Vohra, Shivani& Tu, Khin…[et al.]. 2014. Molecular, Phenotypic Aspects and Therapeutic Horizons of Rare Genetic Bone Disorders. BioMed Research International،Vol. 2014, no. 2014, pp.1-16.
https://search.emarefa.net/detail/BIM-1016435
نمط استشهاد الجمعية الأمريكية للغات الحديثة (MLA)
Faruqi, Taha…[et al.]. Molecular, Phenotypic Aspects and Therapeutic Horizons of Rare Genetic Bone Disorders. BioMed Research International No. 2014 (2014), pp.1-16.
https://search.emarefa.net/detail/BIM-1016435
نمط استشهاد الجمعية الطبية الأمريكية (AMA)
Faruqi, Taha& Dhawan, Naveen& Bahl, Jaya& Gupta, Vineet& Vohra, Shivani& Tu, Khin…[et al.]. Molecular, Phenotypic Aspects and Therapeutic Horizons of Rare Genetic Bone Disorders. BioMed Research International. 2014. Vol. 2014, no. 2014, pp.1-16.
https://search.emarefa.net/detail/BIM-1016435
نوع البيانات
مقالات
لغة النص
الإنجليزية
الملاحظات
Includes bibliographical references
رقم السجل
BIM-1016435
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