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佩尔曼综合征:一例报告,强调其与贝克威思-维德曼综合征和梅干腹综合征的相似性及区别

Perlman syndrome: a case report emphasizing its similarity to and distinction from Beckwith-Wiedemann and prune-belly syndromes.

作者信息

Fahmy J, Kaminsky C K, Parisi M T

机构信息

Children's Hospital Los Angeles, CA 90027, USA.

出版信息

Pediatr Radiol. 1998 Mar;28(3):179-82. doi: 10.1007/s002470050326.

Abstract

Perlman syndrome is a rare entity characterized by hypotonia, facial dysmorphism, gigantism, and visceromegaly including nephromegaly. The current case illustrates the ultrasonographic and computed tomographic appearances of renal abnormalities in this condition. Findings in Perlman syndrome can overlap with and need to be distinguished from two more common clinical entities: prune-belly and Beckwith-Wiedemann syndromes. Additional cranial findings previously unreported are also described.

摘要

佩尔曼综合征是一种罕见的病症,其特征为肌张力减退、面部畸形、巨人症以及包括肾肿大在内的内脏肿大。本病例展示了该病症中肾脏异常的超声和计算机断层扫描表现。佩尔曼综合征的表现可能与另外两种更常见的临床病症重叠,需要加以区分:梅干腹综合征和贝克威思-维德曼综合征。还描述了此前未报告的额外颅脑表现。

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