The Maffucci Syndrome: A Rare Case Report
The Maffucci syndrome is a rare genetic disorder that affects both males and females. It is characterized by a benign tumor of the cartilage (enchondroma), bone deformities, and dark, irregularly shaped hemangiomas. It was first reported by Angelo Maffucci in 1881 -after a forty-year old woman died from complication following amputation of an arm. We are presenting Maffucci syndrome in a 15-year old Ethiopian female. To our knowledge so far, there is no such documented report from Ethiopia.
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Daniel Admassi, Biruk L. WAMISHO (2020-11-24). The Maffucci Syndrome: A Rare Case Report. Ethiopian Journal of Health and Biomedical Sciences, Vol. 2 No. 2 (2010), 3. https://doi.org/10.20372/ejhbs.v2i2.43
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