Richieri-Costa A, Guion-Almeida M L, Pagnan N A
Serviço de Genética Clínica, Hospital de Pesquisa e Reabilitação de Lesões Lábio-Palatais, Universidade de São Paulo, Bauru, Brazil.
Am J Med Genet. 1992 Dec 1;44(6):800-2. doi: 10.1002/ajmg.1320440616.
We report on a Brazilian woman with severe mental retardation, facial and skeletal anomalies characterized by hypertelorism, eye anomalies, broad notched nasal tip, cleft lip, highly arched palate, camptobrachysyndactyly of fingers and toes, and anomalies of the feet. A similarly affected brother died at age one year. The clinical picture strongly suggest the diagnosis of the autosomal recessive acro-fronto-facio-nasal dysostosis syndrome (AFFND). Clinical and genetic aspects are discussed.
我们报告了一名患有严重智力障碍、面部和骨骼异常的巴西女性,其特征为眼距过宽、眼部异常、鼻尖宽阔有缺口、唇裂、高拱腭、手指和脚趾先天性屈曲并指(趾)畸形以及足部异常。一个有类似症状的兄弟在一岁时死亡。临床表现强烈提示为常染色体隐性遗传的肢端-额-面-鼻发育不全综合征(AFFND)。文中讨论了临床和遗传学方面的情况。