103 top medical experts on Genee-Wiedemann syndrome across 8 countries and 4 U.S. states, including 5 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Genee-Wiedemann syndrome: A rare acrofacial dysostosis that is characterized by mandibular and malar hypoplasia, small and cup-shaped ears, lower lid ectropion, and symmetrical postaxial limb deficiencies with absence of the fifth digital rays and ulnar hypoplasia.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Support Organizations
- Foundation for Nager and Miller Syndromes
13210 SE 342nd Street
Auburn, WA 98092
Toll-free: 1-800-507-3667
E-mail: dede@fnms.net
Website: http://www.fnms.net
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- Synonyms: Genee-Wiedemann acrofacial dysostosis, Miller syndrome, POADS syndrome, Postaxial Acrofacial Dysostosis, Postaxial Acrofacial Dysostosis (POADS), Postaxial acrofacial dysostosis (POADS) syndrome, Wildervanck-Smith syndrome
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