Fibrous Dysplasia
What's New
Last Posted: Aug 25, 2024
- Molecular confirmation that fibrocartilaginous dysplasia is a variant of fibrous dysplasia.
Juan Zhou, et al. Journal of clinical pathology 2024 0 - DNA Mutational and Copy Number Variation Profiling of Primary Craniofacial Osteosarcomas by Next-Generation Sequencing.
Gord Guo Zhu, et al. Head and neck pathology 2024 0 (1) 48 - Increased Risk of Breast Cancer at a Young Age in Women with Fibrous Dysplasia.
Majoor Bas Cj, et al. Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2017 0 (1) 84-90 - Increased Prevalence of Malignancies in Fibrous Dysplasia/McCune-Albright Syndrome (FD/MAS): Data from a National Referral Center and the Dutch National Pathology Registry (PALGA).
Hagelstein-Rotman M, et al. Calcified tissue international 2020 11 - Best practice management guidelines for fibrous dysplasia/McCune-Albright syndrome: a consensus statement from the FD/MAS international consortium.
Javaid Muhammad Kassim et al. Orphanet journal of rare diseases 2019 Jun 14(1) 139 - Health-related quality of life and a cost-utility simulation of adults in the UK with osteogenesis imperfecta, X-linked hypophosphatemia and fibrous dysplasia.
Forestier-Zhang Lydia et al. Orphanet journal of rare diseases 2016 11(1) 160 - GNAS Mutations in Fibrous Dysplasia: A Comparative Study of Standard Sequencing and Locked Nucleic Acid PCR Sequencing on Decalcified and Nondecalcified Formalin-fixed Paraffin-embedded Tissues.
Jour George, et al. Applied immunohistochemistry & molecular morphology : AIMM / official publication of the Society for Applied Immunohistochemistry 2015 11 - Detection of SQSTM1/P392L post-zygotic mutations in Paget's disease of bone.
Guay-Bélanger Sabrina, et al. Human genetics 2015 1 (1) 53-65 - The diagnostic utility of the GNAS mutation in patients with fibrous dysplasia: meta-analysis of 168 sporadic cases.
Lee Seung Eun, et al. Human pathology 2012 8 (8) 1234-42 - [Abnormal expression of c-myc, p53, p16 protein and GNAS1 gene mutation in fibrous dysplasia].
Tang Juan, et al. Zhonghua bing li xue za zhi Chinese journal of pathology 2009 5 (5) 292-7
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
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Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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