Which conditions and syndromes involving multiple body parts are included in the differential diagnoses of arthrogryposis multiplex congenita (AMC)?

Updated: Nov 11, 2020
  • Author: Mithilesh Kumar Lal, MD, MBBS, MRCP, FRCPCH, MRCPCH(UK); Chief Editor: Maria Descartes, MD  more...
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Other associated syndromes and conditions include focal femoral dysplasia, hand-muscle wasting and sensorineural deafness, Holt-Oram syndrome, Kuskokwim syndrome, Larsen dysplasia, leprechaunism, megalocornea with multiple skeletal anomalies, Möbius syndrome, nemaline myopathy, oculodentodigital syndrome, ophthalmomandibulomelic dysplasia, orocraniodigital syndrome, otopalatodigital syndrome, Pfeiffer syndrome, Prader-Willi habitus/osteoporosis/hand contractures, pseudothalidomide syndrome, Puretic-Murray syndrome, sacral agenesis, Schwartz-Jampel syndrome, tuberous sclerosis, VATER (vertebral [defects], [imperforate] anus, tracheoesophageal [fistula], radial and renal [dysplasia]) complex, Weaver syndrome, Winchester syndrome, and X-trapezoidocephaly with midfacial hypoplasia and cartilage abnormalities.

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