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| UDK 616-039.38 |
ISSN 035-2899, 39(2014) br.4 p.213-218 |
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Case report Mc Cune-Albright syndrome – case report (Mc Cune-Albright-ov sindrom – prikaz slučaja) Željka Aleksić (1), Aleksandar Aleksić (2) (1) Služba za nuklearnu medicinu, ZC Zaječar, (2) Internistička služba, ZC Zaječar |
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| Download in pdf format | Extended summary:
McCune-Albright syndrome (MAS) is a rare congenital, non-hereditary
benign disease caused by a somatic activating mutation, which occurs
after the formation of the zygote in the gene that encodes the alpha
subunit of the stimulatory G protein (Gs) on chromosome 20q13 and is
characterized by the triad: osteofibrose dysplasia, “cafe-au-lait”
skin pigmentation and various types of endocrinopathies. We report a
case of this rare disease, diagnosed in a woman in the fifth decade
of life, in which changes in the bones were accidentally discovered
at chest radiography as part of the medical examination to obtain a
medical certificate for the employment. Keywords: Mc Cune-Albright syndrome, osteofibrous dysplasia, autonomous hyperthyroidism Napomena: kompletan tekst rada na srpskom jeziku Note: full text in Serbian |
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Corresponding Address: Željka Aleksić Služba za nuklearnu medicinu, Zdravstven Centar Zaječar, Rasadnička bb, 19 000 Zaječar, Srbija; E-mail: lukaal@open.telekom.rs |
Paper received: 10.8.2014 Paper accepted: 10.8.2014 Paper Internet issues: 17.11.2014 |
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