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伊拉帕型脊椎骨骺干骺端骨软骨发育不良。一种伴有短脊柱和跖骨的新型侏儒症

[Irapa type spondylo-epiphyso-metaphyseal osteochondrodysplasia. New type of dwarfism with short spine and metatarsals].

作者信息

Arias S, Mota M

出版信息

Nouv Presse Med. 1976 Feb 7;5(6):319-23.

PMID:1264699
Abstract

A new dwarfism of a spondyloepiphysometaphyseal dysplasia is described among Venezuelan Indians of the Yukpa (Irapa) tribe. Brachyrrhahia, brachymetatarsia and brachyrhyzomelia in upper limbs and manifestations in proximal epiphyses of femora and distal epiphyses of humera, with moderate to serious impairment of gait, but no significance deviations of the spine, are the main clinical findings. It is a well individualized type among a very heterogeneous and ill-defined group of chondrodystrophies. The inheritance is through an autosomal recessive or less probably an X-linked gene.

摘要

在尤帕(伊拉帕)部落的委内瑞拉印第安人中,发现了一种新的脊椎骨骺干骺端发育不良型侏儒症。主要临床症状包括短颈、短跖骨、上肢短肢以及股骨近端骨骺和肱骨远端骨骺的表现,步态有中度至重度受损,但脊柱无明显异常。在一组非常异质且定义不明确的软骨发育不良中,这是一种特征明显的类型。其遗传方式为常染色体隐性遗传,也可能是X连锁基因遗传,但可能性较小。

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