Cenani–Lenz syndrome: A case report

Hayat Al-Nougidan, S. Wani, A. Wafa
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Abstract

Cenani–Lenz syndrome is a rare autosomal recessive congenital malformation syndrome characterized by syndactyly and oligodactyly of fingers and toes, disorganization and fusion of metacarpals, metatarsals, and phalanges, radioulnar synostosis, and mesomelic shortness of the upper limbs, with lower limbs usually being less severely affected and associated with facial dysmorphism and renal abnormality. A case report of a 16-year-old Saudi male presented with four limbs syndactyly of fingers and toes, mild facial dysmorphism, dextroscoliosis, and crossed fused ectopia of the left kidney at the right side is presented here.
Cenani-Lenz综合征1例报告
Cenani-Lenz综合征是一种罕见的常染色体隐性先天性畸形综合征,其特征为手指和脚趾并指和少指,掌骨、跖骨和指骨的组织和融合,尺桡关节闭锁,上肢中膜短,下肢通常受影响较轻,并伴有面部畸形和肾脏异常。一个16岁的沙特男性的病例报告,表现为四肢手指和脚趾并指,轻度面部畸形,右旋脊柱侧凸,左肾交叉融合异位在右侧。
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