ORCID number:Yoshinori Satomura,ORCID number:0000-0002-0083-1774;Corresponding author:Kazuhiko Bessho,MD,PhD,Associate Professor,Department of Pediatrics,Osaka University Graduate School of Medicine,2-2-D5 Yamada-oka,Suita City,Osaka 565-0871,Japan.bessho@ped.med.osaka-u.ac.jp,ORCID number:0000-0003-1684-2213;Taichi Kitaoka,ORCID number:0000-0002-3531-884X;Shinji Takeyari,ORCID number:0000-0002-3627-1932;Yasuhisa Ohata,ORCID number:0000-0001-6084-6620;Takuo Kubota,ORCID number:0000-0003-4483-4405;Keiichi Ozono,ORCID number:0000-0002-6517-8825.
BACKGROUND McCune–Albright syndrome(MAS)is caused by postzygotic somatic mutations of the GNAS gene.It is characterized by the clinical triad of fibrous dysplasia,caféau-lait skin spots,and endocrinological dysfunct...
McCune Albright syndrome is a rare genetic disorder which is characterized by café au lait skin pigmentation, precocious puberty and polyostotic fibrous dysplasia. Treating recurring pathological fractures due to Alb...