Vakili, R., Hashemian, S., Jafarzadeh Esfehani, R., Zare Feizabadi, A. (2019). Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review. International Journal of Pediatrics, 7(5), 9453-9459. doi: 10.22038/ijp.2019.36513.3181
Rahim Vakili; Somayyeh Hashemian; Reza Jafarzadeh Esfehani; Azadeh Zare Feizabadi. "Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review". International Journal of Pediatrics, 7, 5, 2019, 9453-9459. doi: 10.22038/ijp.2019.36513.3181
Vakili, R., Hashemian, S., Jafarzadeh Esfehani, R., Zare Feizabadi, A. (2019). 'Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review', International Journal of Pediatrics, 7(5), pp. 9453-9459. doi: 10.22038/ijp.2019.36513.3181
Vakili, R., Hashemian, S., Jafarzadeh Esfehani, R., Zare Feizabadi, A. Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review. International Journal of Pediatrics, 2019; 7(5): 9453-9459. doi: 10.22038/ijp.2019.36513.3181
Mccune-Albright Syndrome: A Case Report Associated with Pamidronate Therapy and Literature Review
1Department of Pediatric Endocrinology and Metabolism, Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran. AND Medical Genetic Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
2Department of Pediatric Endocrinology and Metabolism, Akbar Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
3Medical Genetic Research Center, Mashhad University of Medical Sciences, Mashhad, Iran.
4Department of Pediatric Endocrinology and Metabolism, Imam Reza Hospital, Faculty of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Abstract
McCune-Albright Syndrome (MAS) is a rare sporadic disease characterized by bone fibrous dysplasia, Café au lait spots and a variable association of hyperfunction endocrine disorders. There is not any certain treatment available for this syndrome, and both physical and emotional disability in these patients is still a major concern for physicians. In present report we have described a 10- year-old girl, presented with precocious puberty, multiple Café au lait macules and fibrous dysplasia, successfully treated with pamidronate in a four-year follow-up period.
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