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A case report of McCune-Albright syndrome with hepatic manifestations
Mohammad Haddadi1, Elahe Lal Kheirkhah2, Mojgan Ansari3
1Department of Nursing Tabas Branch Islamic Azad University Tabas Iran.
Abstract:
McCune-Albright syndrome is a non-hereditary disease characterized by café-au-lait skin spots, fibrous dysplasia of bone, and endocrinopathies. We report a boy with a history of repeated hospitalizations from birth due to severe jaundice and hyperthyroidism. At the age of 2 years, he suffered from a proximal left femoral fracture. During the follow-up, liver function tests were abnormal. Considering the clinical and paraclinical findings, the patient was diagnosed with McCune-Albright syndrome.
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