Arthrogryposis multiplex congenita 3, myogenic type
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Sign InDescription
Myogenic-type arthrogryposis multiplex congenita-3 (AMC3) is an autosomal recessive disorder characterized by decreased fetal movements, hypotonia, variable skeletal defects, including clubfoot and scoliosis, and delayed motor milestones with difficulty walking (summary by Baumann et al., 2017).
Mode of Inheritance
- Autosomal recessive inheritance
VARIANTS
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