Literature DB >> 17375532

Anophthalmos with limb anomalies (Waardenburg opththalmo-acromelic syndrome): report of a new Italian case with renal anomaly and review.

L Garavelli1, S Pedori, R Dal Zotto, F Franchi, M Marinelli, G F Croci, S Bellato, A Ammenti, R Virdis, G Banchini, A Superti-Furga.   

Abstract

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.

Entities:  

Mesh:

Year:  2006        PMID: 17375532

Source DB:  PubMed          Journal:  Genet Couns        ISSN: 1015-8146


  5 in total

1.  Mutations in the SPARC-related modular calcium-binding protein 1 gene, SMOC1, cause waardenburg anophthalmia syndrome.

Authors:  Hana Abouzeid; Gaëlle Boisset; Tatiana Favez; Mohamed Youssef; Iman Marzouk; Nihal Shakankiry; Nader Bayoumi; Patrick Descombes; Céline Agosti; Francis L Munier; Daniel F Schorderet
Journal:  Am J Hum Genet       Date:  2010-12-30       Impact factor: 11.025

2.  SMOC1 is essential for ocular and limb development in humans and mice.

Authors:  Ippei Okada; Haruka Hamanoue; Koji Terada; Takaya Tohma; Andre Megarbane; Eliane Chouery; Joelle Abou-Ghoch; Nadine Jalkh; Ozgur Cogulu; Ferda Ozkinay; Kyoji Horie; Junji Takeda; Tatsuya Furuichi; Shiro Ikegawa; Kiyomi Nishiyama; Satoko Miyatake; Akira Nishimura; Takeshi Mizuguchi; Norio Niikawa; Fumiki Hirahara; Tadashi Kaname; Koh-Ichiro Yoshiura; Yoshinori Tsurusaki; Hiroshi Doi; Noriko Miyake; Takahisa Furukawa; Naomichi Matsumoto; Hirotomo Saitsu
Journal:  Am J Hum Genet       Date:  2010-12-30       Impact factor: 11.025

Review 3.  Hirschsprung's disease and the brain.

Authors:  S W Moore
Journal:  Pediatr Surg Int       Date:  2010-12-05       Impact factor: 1.827

4.  Loss of the BMP antagonist, SMOC-1, causes Ophthalmo-acromelic (Waardenburg Anophthalmia) syndrome in humans and mice.

Authors:  Joe Rainger; Ellen van Beusekom; Jacqueline K Ramsay; Lisa McKie; Lihadh Al-Gazali; Rosanna Pallotta; Anita Saponari; Peter Branney; Malcolm Fisher; Harris Morrison; Louise Bicknell; Philippe Gautier; Paul Perry; Kishan Sokhi; David Sexton; Tanya M Bardakjian; Adele S Schneider; Nursel Elcioglu; Ferda Ozkinay; Rainer Koenig; Andre Mégarbané; C Nur Semerci; Ayesha Khan; Saemah Zafar; Raoul Hennekam; Sérgio B Sousa; Lina Ramos; Livia Garavelli; Andrea Superti Furga; Anita Wischmeijer; Ian J Jackson; Gabriele Gillessen-Kaesbach; Han G Brunner; Dagmar Wieczorek; Hans van Bokhoven; David R Fitzpatrick
Journal:  PLoS Genet       Date:  2011-07-07       Impact factor: 5.917

5.  Congenital anophthalmia and microphthalmia: epidemiology and orbitofacial rehabilitation.

Authors:  Sara Llorente-González; J Peralta-Calvo; J M Abelairas-Gómez
Journal:  Clin Ophthalmol       Date:  2011-12-13
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.