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Case Reports in Genetics
Volume 2017, Article ID 9327169, 5 pages
https://doi.org/10.1155/2017/9327169
Case Report

Freeman–Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa

1Department of Paediatrics and Child Health, Kilimanjaro Christian Medical Centre, P.O. Box 3010, Moshi, Tanzania
2Department of Human Genetics, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525 GA Nijmegen, Netherlands
3Department of Neurology, Radboud University Medical Center, Geert Grooteplein Zuid 10, 6525 GA Nijmegen, Netherlands

Correspondence should be addressed to M. C. J. Dekker; moc.stewz@ekeiram

Received 27 October 2016; Accepted 6 April 2017; Published 11 May 2017

Academic Editor: Shoji Ichikawa

Copyright © 2017 A. M. Ali et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

A. M. Ali, R. M. Mbwasi, G. Kinabo, E.-J. Kamsteeg, B. C. Hamel, and M. C. J. Dekker, “Freeman–Sheldon Syndrome: First Molecularly Confirmed Case from Sub-Saharan Africa,” Case Reports in Genetics, vol. 2017, Article ID 9327169, 5 pages, 2017. https://doi.org/10.1155/2017/9327169.