Diagnostic workup in children with arthrogryposis: description of practices from a single reference centre, comparison with literature and suggestion of recommendations.

Journal of medical genetics(2023)

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摘要
The aetiological management for patients with AMC remains arduous. This process will be facilitated by the increasing use of next-generation sequencing combined with detailed phenotyping. Invasive investigations should be avoided because of their limited yield.
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关键词
amyoplasia,arthrogryposis multiplex congenita,diagnosis,genetics,medical,neuromuscular diseases,pediatrics
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