Poland Syndrome

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Poland Syndrome

An autosomal dominant [MIM 173800] condition—which may be a developmental field defect, or sequence—which is characterised by unilateral hypoplasia of skeletal muscle in the shoulder and chest wall, affecting the pectoralis major, serratus anterior, latissimus dorsi, variable hypoplasia of ribs, hand or entire arm, or ipsilateral syndactyly; most cases are de novo mutations

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