Gutiérrez-Amavizca B E, Juárez-Vázquez C I, Orozco-Castellanos R, Arnaud L, Macías-Gómez N M, Barros-Nuñez P
División de Genética, Centro de Investigación Biomédica de Occidente, Instituto Mexicano del Seguro Social, Guadalajara, Jalisco, México.
Genet Couns. 2013;24(2):185-91.
Megalocornea can be observed as an isolated abnormality that is inherited by an X-linked mechanism, or it can be associated with other entities. Megalocornea-mental retardation syndrome, also known as Neuhauser syndrome, is a rare autosomal recessive congenital disorder that presents with megalocornea, mental retardation, hypotonia, and facial dysmorphism, among other signs. With the report of this new case, and after an extensive review of the literature, we attempt to delineate the Neuhauser syndrome phenotype.
巨角膜可表现为一种通过X连锁机制遗传的孤立性异常,也可与其他病症相关。巨角膜-智力发育迟缓综合征,也称为诺伊豪泽综合征,是一种罕见的常染色体隐性先天性疾病,其表现包括巨角膜、智力发育迟缓、肌张力减退和面部畸形等症状。随着这例新病例的报告,并在对文献进行广泛回顾之后,我们试图描述诺伊豪泽综合征的表型。