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McCune-albright syndrome: report of a case
Iranian Journal of Nuclear Medicine. 2010; 18 (1): 57-61
em Inglês | IMEMR | ID: emr-132096
ABSTRACT
A 29-year old female with bone pain and history of precocious puberty was referred for bone scintigraphy. On physical examination caf‚ au lait macular spots were noted on her neck, buttocks and left leg. Bone scan showed multiple areas of intense increased activity which was in favour of polyostotic fibrous dysplasia. Considering the presence of polyostotic fibrous dysplasia, precocious puberty and caf‚ au lait macular spots, MacCune-Albright syndrome was confirmed in this patient
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Índice: IMEMR (Mediterrâneo Oriental) Idioma: Inglês Revista: Iran. J. Nucl. Med. Ano de publicação: 2010

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Índice: IMEMR (Mediterrâneo Oriental) Idioma: Inglês Revista: Iran. J. Nucl. Med. Ano de publicação: 2010