Duane anomaly, congenital myopathy and severe scoliosis in sibs: new AR syndrome?

Alain Verloes , Jean-Paul Misson , Philippe Gillet , Clarisse Baumann , Micheline Spiritus , Manuel Deprez
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Abstract

We report on two sisters who show a similar pattern of anomalies consisting of bilateral Stilling–Türk–Duane retraction syndrome (type 3), non-progressive hypotonia with delayed motor milestones but normal intelligence, severe, early onset scoliosis, and short stature. Muscular biopsy revealed numerous regenerating fibers, but no specific abnormalities among the non-regenerating fibers. This combination of anomalies has not been previously reported, and could represent a new autosomal recessive syndrome. The only differential diagnosis is Crisfield–Dretakis–Sharpe syndrome, a combination of lateral gaze palsy, ptosis, and scoliosis without hypotonia, recessively inherited.

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兄弟姐妹中Duane异常、先天性肌病和严重脊柱侧凸:新的AR综合征?
我们报告了两名姐妹,她们表现出类似的异常模式,包括双侧stillling - t rk - duane后缩综合征(3型),非进行性张力低下伴运动里程碑延迟,但智力正常,严重的早发性脊柱侧凸和身材矮小。肌肉活检显示大量再生纤维,但非再生纤维未见特殊异常。这种异常的组合以前没有报道过,可能代表一种新的常染色体隐性综合征。唯一的鉴别诊断是Crisfield-Dretakis-Sharpe综合征,这是一种隐性遗传的组合,包括侧视麻痹、上睑下垂和脊柱侧凸,但无强直。
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