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骨硬化症综述。

A review of the osteopetroses.

作者信息

Beighton P, Horan F, Hamersma H

出版信息

Postgrad Med J. 1977 Aug;53(622):507-16. doi: 10.1136/pgmj.53.622.507.

Abstract

The osteopetroses are a group of conditions which are characterized by varying combinations of bony sclerosis and modelling defects. Classical osteopetrosis may be inherited as an autosomal dominant or autosomal recessive: the former variety is benign, heterogeneous and comparatively common, while the latter is precocious, potentially lethal and rare. Many other craniotubular dysplasias and hyperostoses are loosely grouped with the osteopetroses. The commonest of these is the autosomal dominant form of craniometaphyseal dysplasia, while the others which are well known include Pyle disease, and van Buchem disease. Sclerosteosis is a progressive condition in which massive cranial thickening is associated with syndactyly and gigantism. Each of these disorders has specific clinical and radiographic features, which permit recognition. Diagnostic accuracy is crucial for treatment, prognostication and effective genetic management.

摘要

骨硬化症是一组以骨硬化和塑形缺陷的不同组合为特征的病症。典型的骨硬化症可呈常染色体显性或常染色体隐性遗传:前者为良性、异质性且相对常见,而后者发病早、有潜在致命性且罕见。许多其他颅管发育异常和骨质增生与骨硬化症被大致归为一类。其中最常见的是常染色体显性形式的颅骨干骺端发育异常,而其他知名的病症包括派尔病和范布赫姆病。骨肥厚性骨病是一种进行性病症,其特征为颅骨大量增厚并伴有并指(趾)畸形和巨人症。这些病症中的每一种都有特定的临床和影像学特征,有助于识别。诊断准确性对于治疗、预后评估和有效的遗传管理至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/beeb/2496745/3442f6255d6c/postmedj00272-0089-a.jpg

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