Review for "A signature of circulating miRNAs associated with Fibrous Dysplasia of bone: the mirDys study"

2020 ◽  
Author(s):  
M.A. Legrand ◽  
M. Millet ◽  
B. Merle ◽  
JC. Rousseau ◽  
A. Hemmendinger ◽  
...  

Metabolism ◽  
1968 ◽  
Vol 17 (11) ◽  
pp. 988-998 ◽  
Author(s):  
Will G. Ryan ◽  
Albert F. Nibbe ◽  
Theodore B. Schwartz ◽  
Robert D. Ray

2012 ◽  
Vol 7 (Suppl 1) ◽  
pp. S3 ◽  
Author(s):  
Roland D Chapurlat ◽  
Deborah Gensburger ◽  
Juan M Jimenez-Andrade ◽  
Joseph R Ghilardi ◽  
Marilyn Kelly ◽  
...  

2018 ◽  
Vol 85 (6) ◽  
pp. 1169-1179 ◽  
Author(s):  
Marlous Rotman ◽  
Neveen Agnes Therese Hamdy ◽  
Natasha M. Appelman‐Dijkstra

1957 ◽  
Vol 234 (4) ◽  
pp. 590-606 ◽  
Author(s):  
MARVIN L. DAVES ◽  
JOHN H. YARDLEY

2018 ◽  
Author(s):  
Jinrong Zhao ◽  
Jinguo Yu

Abstract Background: McCune-Albright syndrome (MAS) is a rare disease defined by the triad of polyostotic fibrous dysplasia of bone, skin spots, and precocious puberty. No available treatment is effective in changing the course of fibrous dysplasia of bone, but symptomatic patients require the rapeutic support to reduce bone pain and prevent fractures and deformities.we reported 1 case of McCune-Albright syndrome with exophthalmos in clinical practice. Case presentation:A 35-year-old female was admitted to our hospital who complained about “skin pigmentation for 35 years, vaginal bleeding for 30 years and progressive skeletal deformity for 28 years and exophthalmos for 2 years. And after the examination, she was been diagnosed with“McCune-Albright syndrome with exophthalmos”.We highlighted the pathogenesis and development of the disease in this rare condition. Conclusion: McCune-Albright syndrome with exophthalmos due to multiple fibrous dysplasia is rare but can be seen in clinical practice.


1997 ◽  
Vol 38 (3) ◽  
pp. 368-371 ◽  
Author(s):  
M. Court-Payen ◽  
L. Ingemann Jensen ◽  
B. Bjerregaard ◽  
G. Schwarz Lausten ◽  
B. Skjoldbye

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