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五名男性患者的哈特斯菲尔德前脑无裂畸形-缺指(趾)畸形综合征:进一步描述与综述

Hartsfield holoprosencephaly-ectrodactyly syndrome in five male patients: further delineation and review.

作者信息

Vilain Catheline, Mortier Geert, Van Vliet Guy, Dubourg Christèle, Heinrichs Claudine, de Silva Deephti, Verloes Alain, Baumann Clarisse

机构信息

Service de Génétique Médicale, ULB, Hôpital Erasme, Brussels, Belgium.

出版信息

Am J Med Genet A. 2009 Jul;149A(7):1476-81. doi: 10.1002/ajmg.a.32678.

Abstract

We report on five male subjects with a triad of signs compatible with Hartsfield syndrome: ectrodactyly, holoprosencephaly, and mental retardation. Only six patients with this distinctive association have been reported over the past 20 years, all of them being males. Of the patients described here, some have unreported findings such as vermian hypoplasia in one and prolonged survival into adulthood in two. Two patients developed central diabetes insipidus. All were mentally retarded. No abnormalities were found at the cytogenetic level, including array CGH in two. No known genes for holoprosencephaly or ectrodactyly were found, including GLI2. The cause of Hartsfield syndrome is unknown. An X-linked defect is possible, although no recurrences have been described to date. Our observations almost double the number of cases. They underscore the usefulness of fetal brain imaging in the differential diagnosis of syndromal clefting diagnosed in utero, particularly when ectrodactyly-ectodermal dysplasia-clefting syndrome is suspected.

摘要

我们报告了五名男性患者,他们具有与哈茨菲尔德综合征相符的三联征:缺指(趾)畸形、前脑无裂畸形和智力障碍。在过去20年中,仅有六例具有这种独特关联的患者被报道,均为男性。在此描述的患者中,一些有未报道的发现,如其中一例有蚓部发育不全,两例存活至成年期。两名患者出现中枢性尿崩症。所有患者均有智力障碍。在细胞遗传学水平未发现异常,包括两例的阵列比较基因组杂交。未发现与前脑无裂畸形或缺指(趾)畸形相关的已知基因,包括GLI2。哈茨菲尔德综合征的病因尚不清楚。尽管迄今为止尚未描述有复发情况,但可能存在X连锁缺陷。我们的观察结果使病例数几乎增加了一倍。它们强调了胎儿脑部成像在宫内诊断的综合征性腭裂鉴别诊断中的有用性,特别是在怀疑为缺指(趾)-外胚层发育不良-腭裂综合征时。

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