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与家族性青少年肾单位肾痨及手部锥形骨骺相关的莱伯先天性黑矇(萨尔迪诺-梅恩泽尔综合征)

Leber's congenital amaurosis associated with familial juvenile nephronophthisis and cone-shaped epiphyses of the hands (the Saldino-Mainzer syndrome).

作者信息

Ellis D S, Heckenlively J R, Martin C L, Lachman R S, Sakati N A, Rimoin D L

出版信息

Am J Ophthalmol. 1984 Feb;97(2):233-9. doi: 10.1016/s0002-9394(14)76095-7.

Abstract

Three affected children (a 13-year-old girl and her 7- and 8-year-old brothers) in a sibship of eight had findings consistent with the Saldino-Mainzer syndrome (skeletal dysplasia associated with Leber's congenital amaurosis, familial juvenile nephronophthisis, and cone-shaped epiphyses of the hands). Two also had pigmented midline nevi. Although tapetoretinal degeneration and familial juvenile nephronophthisis are associated in the inherited Senior-Loken syndrome, the rare association of these abnormalities with cone-shaped epiphyses of the hands suggested an autosomal recessive syndrome with variable expression remarkably similar to the Saldino-Mainzer syndrome, which may or may not be distinct from the Senior-Loken syndrome. The association of tapetoretinal degeneration with skeletal dysplasia may indicate asymptomatic renal or hepatic disease.

摘要

一个八口之家的三个患病儿童(一名13岁女孩及其7岁和8岁的弟弟)有与萨尔迪诺-迈泽综合征相符的表现(一种与莱伯先天性黑矇、家族性青少年肾单位肾痨以及手部锥形骨骺相关的骨骼发育异常)。其中两人还患有色素沉着性中线痣。虽然视网膜色素变性和家族性青少年肾单位肾痨在遗传性的Senior-Loken综合征中相关联,但这些异常与手部锥形骨骺的罕见关联提示了一种常染色体隐性综合征,其表现多样,与萨尔迪诺-迈泽综合征极为相似,可能与Senior-Loken综合征不同,也可能并无区别。视网膜色素变性与骨骼发育异常的关联可能提示无症状的肾脏或肝脏疾病。

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