D. Mccune, Osteitis fibrosa cystica: the case of a nine-year-old girl who also exhibits precocious puberty, multiple pigmentation of the skin and hyperthyroidism, Am J Dis Child, vol.52, pp.743-744, 1936.

F. Albright, A. Butler, A. Hampton, and P. Smith, Syndrome Characterized by Osteitis Fibrosa Disseminata, Areas of Pigmentation and Endocrine Dysfunction, with Precocious Puberty in Females, New England Journal of Medicine, vol.216, issue.17, pp.727-746, 1937.
DOI : 10.1056/NEJM193704292161701

M. Zacharin, The spectrum of McCune Albright syndrome, Pediatr Endocrinol Rev, vol.4, issue.4, pp.412-420, 2007.

C. Dumitrescu and M. Collins, McCune-Albright syndrome, Orphanet Journal of Rare Diseases, vol.3, issue.1, p.12, 2008.
DOI : 10.1186/1750-1172-3-12

T. Völkl and H. Dörr, McCune-Albright Syndrome: Clinical Picture and Natural History in Children and Adolescents, Journal of Pediatric Endocrinology and Metabolism, vol.145, issue.Supplement, 2006.
DOI : 10.1016/j.jpeds.2004.06.083

P. Chanson, S. Salenave, and P. Orcel, McCune-Albright syndrome in adulthood

A. Morelli, M. Marini, R. Mancina, M. Luconi, L. Vignozzi et al., Sex Steroids and Leptin Regulate the ???First Kiss??? (KiSS 1/G-Protein-Coupled Receptor 54 System) in Human Gonadotropin-Releasing-Hormone-Secreting Neuroblasts, The Journal of Sexual Medicine, vol.5, issue.5, pp.1097-113, 2008.
DOI : 10.1111/j.1743-6109.2008.00782.x

G. Hausman, C. Barb, and C. Lents, Leptin and reproductive function, Biochimie, vol.94, issue.10, pp.2075-81, 2012.
DOI : 10.1016/j.biochi.2012.02.022

W. Marshall and J. Tanner, Variations in pattern of pubertal changes in girls., Archives of Disease in Childhood, vol.44, issue.235, pp.291-303, 1969.
DOI : 10.1136/adc.44.235.291

W. Marshall and J. Tanner, Variations in the Pattern of Pubertal Changes in Boys, Archives of Disease in Childhood, vol.45, issue.239
DOI : 10.1136/adc.45.239.13

J. Fuqua, Treatment and Outcomes of Precocious Puberty: An Update, The Journal of Clinical Endocrinology & Metabolism, vol.98, issue.6, pp.2198-207
DOI : 10.1210/jc.2013-1024

E. Giabicani, S. Allali, A. Durand, J. Sommet, A. Couto-silva et al., Presentation of 493 Consecutive Girls with Idiopathic Central Precocious Puberty: A Single-Center Study, PLoS ONE, vol.123, issue.7, p.70931, 2013.
DOI : 10.1371/journal.pone.0070931.t003

M. Berbero?lu, Precocious Puberty and Normal Variant Puberty: Definition, etiology, diagnosis and current management - Review, Journal of Clinical Research in Pediatric Endocrinology, vol.1, issue.4, pp.164-74, 2009.
DOI : 10.4274/jcrpe.v1i4.3

P. Matarazzo, R. Lala, M. Andreo, S. Einaudi, F. Altare et al., Study Group for Gs alpha Protein Related Diseases of the Italian Society for Pediatric Endocrinology and Diabetes. McCune-Albright syndrome: persistence of autonomous ovarian hyperfunction during adolescence and earlyadult age, J Pediatr Endocrinol Metab, vol.19, issue.2, pp.607-624, 2006.

L. Gaspari, F. Paris, M. Nicolino, F. Hameury, H. Bonnaure et al., Fetal ovarian cysts: an early manifestation of McCune-Albright syndrome? Prenat Diagn, pp.859-63, 2012.

A. Boyce, W. Chong, T. Shawker, P. Pinto, W. Linehan et al., Characterization and Management of Testicular Pathology in McCune-Albright Syndrome, The Journal of Clinical Endocrinology & Metabolism, vol.97, issue.9, pp.1782-90, 2012.
DOI : 10.1210/jc.2012-1791

J. Mieszczak and E. Eugster, Treatment of precocious puberty in McCune-Albright syndrome, Pediatr Endocrinol Rev, vol.4, pp.419-441, 2007.

D. Cremoux and P. , Aromatase inhibitors: pharmacological aspects, Bull Cancer, vol.87, pp.23-29, 2000.

M. Riminucci, P. Robey, and P. Bianco, The pathology of fibrous dysplasia and the McCune-Albright syndrome, Pediatr Endocrinol Rev, vol.4, pp.401-412, 2007.

J. Lee, E. Fitzgibbon, Y. Chen, H. Kim, L. Lustig et al., Clinical guidelines for the management of craniofacial fibrous dysplasia, Orphanet Journal of Rare Diseases, vol.7, issue.Suppl 1, p.2, 2012.
DOI : 10.1186/1750-1172-7-S1-S2

A. Leet, C. Chebli, H. Kushner, C. Chen, M. Kelly et al., Fracture Incidence in Polyostotic Fibrous Dysplasia and the McCune-Albright Syndrome, Journal of Bone and Mineral Research, vol.22, issue.4, 2004.
DOI : 10.2106/00004623-198769030-00012

A. Leet, E. Magur, J. Lee, S. Wientroub, P. Robey et al., Fibrous Dysplasia in the Spine, The Journal of Bone & Joint Surgery, vol.86, issue.3, pp.531-538, 2004.
DOI : 10.2106/00004623-200403000-00011

F. Mancini, A. Corsi, D. Maio, F. Riminucci, M. Ippolito et al., Scoliosis and spine involvement in fibrous dysplasia of bone, European Spine Journal, vol.4, issue.2, pp.196-202, 2009.
DOI : 10.1056/NEJM199112123252403

P. Ruggieri, F. Sim, J. Bond, and K. Unni, Malignancies in fibrous dysplasia. Cancer, pp.1411-1435, 1994.

C. Defilippi, D. Chiappetta, D. Marzari, A. Mussa, and R. Lala, Image Diagnosis in McCune-Albright Syndrome, Journal of Pediatric Endocrinology and Metabolism, vol.14, issue.Supplement, pp.561-70, 2006.
DOI : 10.1046/j.1354-523X.2003.00971.x

. Mccune-albright, Syndrome: intensely hypermetabolic polyostotic fibrous dysplasia on F-18 FDG-PET, Clin Nucl Med, vol.34, issue.11, pp.795-802, 2009.

E. Ippolito, E. Bray, A. Corsi, D. Maio, F. Exner et al., Natural history and treatment of fibrous dysplasia of bone: a multicenter clinicopathologic study promoted by the European Pediatric Orthopaedic Society, J Pediatr Orthop B, vol.12, issue.3, pp.155-77, 2003.

M. Zacharin, O. Sullivan, and M. , Intravenous pamidronate treatment of polyostotic fibrous dysplasia associated with the McCune Albright syndrome, The Journal of Pediatrics, vol.137, issue.3, pp.403-412, 2000.
DOI : 10.1067/mpd.2000.107836

K. Shah, The diagnostic and clinical significance of café-au-lait macules. Pediatr Clin North Am, pp.1131-53, 2010.

M. Collins, F. Singer, and E. Eugster, McCune-Albright syndrome and the extraskeletal manifestations of fibrous dysplasia, Orphanet Journal of Rare Diseases, vol.7, issue.Suppl 1, 2012.
DOI : 10.1186/1750-1172-7-S1-S4

G. Mastorakos, N. Mitsiades, A. Doufas, and D. Koutras, Hyperthyroidism in McCune-Albright Syndrome with a Review of Thyroid Abnormalities Sixty Years After the First Report, Thyroid, vol.7, issue.3, pp.433-442, 1997.
DOI : 10.1089/thy.1997.7.433

D. Tessaris, A. Corrias, P. Matarazzo, D. Sanctis, L. Wasniewska et al., Thyroid Abnormalities in Children and Adolescents with McCune-Albright Syndrome, Hormone Research in Paediatrics, vol.78, issue.3, pp.151-158, 2012.
DOI : 10.1159/000342641

P. Chanson, A. Dib, A. Visot, and P. Derome, McCune-Albright syndrome and acromegaly: clinical studies and responses to treatment in five cases, European Journal of Endocrinology, vol.131, issue.3, pp.229-263, 1994.
DOI : 10.1530/eje.0.1310229

R. Brown, M. Kelly, and M. Collins, Cushing Syndrome in the McCune-Albright Syndrome, The Journal of Clinical Endocrinology & Metabolism, vol.95, issue.4, pp.1508-1523
DOI : 10.1210/jc.2009-2321

L. Weinstein, A. Shenker, P. Gejman, M. Merino, E. Friedman et al., Activating Mutations of the Stimulatory G Protein in the McCune???Albright Syndrome, New England Journal of Medicine, vol.325, issue.24, pp.1688-95, 1991.
DOI : 10.1056/NEJM199112123252403

M. Riminucci, I. Saggio, P. Robey, and P. Bianco, Fibrous Dysplasia as a Stem Cell Disease, Journal of Bone and Mineral Research, vol.303, issue.Suppl 1, pp.125-156, 2006.
DOI : 10.1126/science.1088757

URL : http://onlinelibrary.wiley.com/doi/10.1359/jbmr.06s224/pdf

. Mccune-albright, syndrome in a discordant monozygotic twin, Isr Med Assoc J, vol.11, issue.6, pp.343-350, 2009.

L. Weinstein, S. Yu, D. Warner, and J. Liu, Endocrine manifestations of stimulatory G protein alpha-subunit mutations and the role of genomic imprinting, Endocr Rev, vol.22, issue.5, pp.675-705, 2001.

S. Narumi, K. Matsuo, T. Ishii, Y. Tanahashi, and T. Hasegawa, Quantitative and Sensitive Detection of GNAS Mutations Causing McCune-Albright Syndrome with Next Generation Sequencing, PLoS ONE, vol.365, issue.3, p.60525, 2013.
DOI : 10.1371/journal.pone.0060525.t001

D. Lu, C. Haskell-luevano, D. Vage, and R. Cone, Functional variants of the MSH Receptor, Agouti, and their effects in mammalian pignmentation. G Proteins, receptors, and disease, pp.231-259, 1998.

P. Sassone-corsi, Signaling pathways and c-fos transcriptional responses-links to inherited diseases, N Engl J Med Jun, vol.8332, issue.23, pp.1576-1583, 1995.
DOI : 10.1056/nejm199506083322311

S. Subbiah, G. Palikhe, S. Bhadada, K. Mukherjee, and A. Bhansali, Acrogigantism and facial asymmetry: McCune-Albright syndrome, Journal of Pediatric Endocrinology and Metabolism, vol.228, issue.9-10, pp.9-10835, 2011.
DOI : 10.1210/jc.2005-0311

A. Rahman, S. Madge, K. Billing, P. Anderson, I. Leibovitch et al., Craniofacial fibrous dysplasia: clinical characteristics and long-term outcomes, Eye, vol.51, issue.12, pp.2175-81, 2009.
DOI : 10.1002/1097-0142(19940301)73:5<1411::AID-CNCR2820730516>3.0.CO;2-T

URL : http://www.nature.com/eye/journal/v23/n12/pdf/eye20096a.pdf

P. Chanson, S. Salenave, and J. Young, Ovarian dysfunction by activating mutation of GS alpha: McCune-Albright syndrome as a model, Annales d'Endocrinologie, vol.71, issue.3
DOI : 10.1016/j.ando.2010.02.015

P. Feuillan, C. Foster, O. Pescovitz, K. Hench, T. Shawker et al., Treatment of Precocious Puberty in the McCune???Albright Syndrome with the Aromatase Inhibitor Testolactone, New England Journal of Medicine, vol.315, issue.18, pp.1115-1124, 1986.
DOI : 10.1056/NEJM198610303151802

D. Liens, P. Delmas, and P. Meunier, Long-term effects of intravenous pamidronate in fibrous dysplasia of bone, The Lancet, vol.343, issue.8903, pp.953-957, 1994.
DOI : 10.1016/S0140-6736(94)90069-8

C. Stratakis, Cushing Syndrome in Pediatrics, Endocrinology and Metabolism Clinics of North America, vol.41, issue.4, pp.793-803, 2012.
DOI : 10.1016/j.ecl.2012.08.002