Lacombe D, Creusot G, Battin J
Clinique de Pédiatrie et Génétique Médicale, Hôpital des Enfants, Bordeaux, France.
Am J Med Genet. 1992 Feb 1;42(3):374-6. doi: 10.1002/ajmg.1320420325.
A new syndrome was identified by Toriello and Carey (Am J Med Genet 31:17-23, 1988), based on the description of four children, three of whom were sibs. The main manifestations included agenesis of the corpus callosum, telecanthus, short palpebral fissures, small nose with anteverted nares, retrognathia, abnormal ears, laryngeal and cardiac anomalies, brachydactyly, and hypotonia. We describe findings in a patient, presumed to be another case of the Toriello-Carey syndrome, which extend the phenotype of the syndrome.
托列洛和凯里(《美国医学遗传学杂志》31:17 - 23,1988年)根据对4名儿童的描述确定了一种新综合征,其中3名儿童为同胞。主要表现包括胼胝体发育不全、眼距增宽、睑裂短小、鼻孔前倾的小鼻子、下颌后缩、耳部异常、喉和心脏异常、短指畸形以及肌张力减退。我们描述了一名患者的发现,推测该患者为托列洛 - 凯里综合征的另一病例,这扩展了该综合征的表型。