Mandibulofacial Dysostosis

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When Her Son Was Diagnosed with MFDM, She Couldn’t Find A Community. So She Helped Build One.

Post author:Sunniva Bean
Post published:March 10, 2020
Post category:Microcephaly Rare Disease

As originally reported in the Cincinnati Children's, Brittney writes how she came into the world of rare diseases when her and her husband Michael decided to adopt a baby who…

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