The Maffucci Syndrome: A Rare Case Report

Authors

  • Daniel Admassi
  • Biruk L. WAMISHO

DOI:

https://doi.org/10.20372/ejhbs.v2i2.43

Abstract

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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Published

2020-11-24

How to Cite

1.
Daniel Admassi, Biruk L. WAMISHO. The Maffucci Syndrome: A Rare Case Report. Ethiop J Health Biomed Sci [Internet]. 2020 Nov. 24 [cited 2024 Apr. 26];2(2):3. Available from: https://journal.uog.edu.et/index.php/EJHBS/article/view/43

Issue

Section

Case Report