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先天性鱼鳞病、毛囊性皮肤萎缩、毛发稀少和少汗症:一种新的遗传性皮肤病?

Congenital ichthyosis, follicular atrophoderma, hypotrichosis, and hypohidrosis: a new genodermatosis?

作者信息

Lestringant G G, Küster W, Frossard P M, Happle R

机构信息

Tawam Hospital, Al Ain, United Arab Emirates.

出版信息

Am J Med Genet. 1998 Jan 13;75(2):186-9. doi: 10.1002/(sici)1096-8628(19980113)75:2<186::aid-ajmg12>3.0.co;2-l.

Abstract

Follicular atrophoderma is a rare anomaly observed mainly in the X-dominant form of chondrodysplasia punctata (Conradi-Hünermann-Happle syndrome) and in the X-linked dominant Bazex syndrome. We report on five Emirati sibs (three girls and two boys), 4-18 years old, with normal stature, diffuse congenital ichthyosis, patchy follicular atrophoderma, generalized and diffuse non-scarring hypotrichosis, and marked hypohidrosis. Steroid sulfatase activity, assessed in the two boys, was found to be normal. Electron microscopic studies of ichthyotic skin did not show any specific abnormality. The association of congenital diffuse ichthyosis with follicular atrophoderma and hypotrichosis has not been reported before. The patients were reminiscent of Bazex syndrome; however, ichthyosis is not a component of Bazex syndrome. We conclude that this syndrome of congenital ichthyosis with follicular atrophoderma represents a new autosomal recessive genodermatosis.

摘要

毛囊性皮肤萎缩症是一种罕见的异常情况,主要见于X连锁显性型点状软骨发育不良(康拉迪-许纳曼-哈普尔综合征)和X连锁显性巴泽克斯综合征。我们报告了5名阿联酋同胞(3名女孩和2名男孩),年龄在4至18岁之间,身材正常,患有弥漫性先天性鱼鳞病、片状毛囊性皮肤萎缩症、全身性和弥漫性非瘢痕性毛发稀少症以及明显的少汗症。对两名男孩进行的类固醇硫酸酯酶活性评估发现其正常。对鱼鳞病皮肤进行的电子显微镜研究未显示任何特异性异常。先天性弥漫性鱼鳞病与毛囊性皮肤萎缩症和毛发稀少症的关联此前未见报道。这些患者让人联想到巴泽克斯综合征;然而,鱼鳞病并非巴泽克斯综合征的组成部分。我们得出结论,这种伴有毛囊性皮肤萎缩症的先天性鱼鳞病综合征代表一种新的常染色体隐性遗传性皮肤病。

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