Garavelli L, Pedori S, Dal Zotto R, Franchi F, Marinelli M, Croci G F, Bellato S, Ammenti A, Virdis R, Banchini G, Superti-Furga A
Department of Pediatrics and Genetic Unit, S. Maria Nuova Hospital, Reggio Emilia, Italy.
Genet Couns. 2006;17(4):449-55.
Anophthalmos with limb anomalies (Waardenburg Opththalmo-Acromelic Syndrome) is a very rare autosomal recessive multiple congenital anomaly syndrome, first described by Waardenburg et al. in 1961 (MIM 206920). It is characterized by mono or more often bilateral anophthalmia/microphthalmia and foot malformations, which can be observed in 91% of the patients. The most common anomaly of the feet is the presence of four toes. The hands are affected bilaterally in 77% of the cases. The most characteristic anomaly is the synostosis of the fourth and fifth metacarpals. To date, 33 cases from 19 families have been reported. We present an Italian case of anophthalmia with limb anomalies and a renal malformation, which has never been described in the literature.
无眼畸形合并肢体异常(瓦尔登堡眼-肢端发育不全综合征)是一种极为罕见的常染色体隐性多发性先天性异常综合征,于1961年由瓦尔登堡等人首次描述(MIM 206920)。其特征为单眼或更常见的双眼无眼畸形/小眼畸形以及足部畸形,91%的患者可观察到这些症状。足部最常见的异常是有四个脚趾。77%的病例双手双侧受累。最具特征性的异常是第四和第五掌骨融合。迄今为止,已报道了来自19个家庭的33例病例。我们报告一例意大利籍无眼畸形合并肢体异常及肾脏畸形的病例,该病例在文献中从未被描述过。