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颅指综合征:1例菲利皮综合征患儿报告及鉴别诊断讨论

Craniodigital syndromes: report of a child with Filippi syndrome and discussion of differential diagnosis.

作者信息

Toriello H V, Higgins J V

机构信息

Genetics Services, Butterworth Hospital, Grand Rapids, Michigan, USA.

出版信息

Am J Med Genet. 1995 Jan 16;55(2):200-4. doi: 10.1002/ajmg.1320550210.

Abstract

We describe a boy with low birth weight, congenital microcephaly, multiple minor facial anomalies, cleft palate, soft tissue syndactyly of fingers and toes, and moderate to severe mental retardation. Literature review suggested 6 possible diagnoses, including Scott craniodigital syndrome, Chitayat syndrome, Filippi syndrome, Zerres syndrome, Kelly syndrome, and Woods syndrome. Each has as part of the phenotype craniofacial anomalies and soft tissue syndactyly of fingers and toes; and superficially, distinction among the 6 may be difficult. However, based on the phenotype analysis we performed, we conclude that our patient has Filippi syndrome, and thus is the first reported case from the United States.

摘要

我们描述了一名低出生体重、先天性小头畸形、多种轻微面部异常、腭裂、手指和脚趾软组织并指(趾)以及中度至重度智力发育迟缓的男孩。文献综述提出了6种可能的诊断,包括斯科特颅指综合征、奇塔亚特综合征、菲利皮综合征、泽雷斯综合征、凯利综合征和伍兹综合征。每种综合征的表型都包括颅面异常以及手指和脚趾的软组织并指(趾);从表面上看,这6种综合征可能难以区分。然而,基于我们进行的表型分析,我们得出结论,我们的患者患有菲利皮综合征,因此是美国首例报告病例。

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