Arthrogryposis multiplex congenita: A report of two cases

James G. Brooks, Douglas J. Coster

Research output: Contribution to journalArticlepeer-review

4 Citations (Scopus)

Abstract

Arthrogryposis multiplex congenita refers to a group of birth defects characterised by multiple joint contractures. The syndrome is caused by neuropathic disease, myopathic disease, or any other cause of decreased fetal joint mobility. Multiple and usually symmetric joint abnormalities with associated muscular and soft tissue hypoplasia are noted at birth. A variety of associated congenital anomalies affecting many organ systems are frequently found. Ocular and orbital findings have been described in patients with arthrogryposis but corneal disease has only rarely been reported. We present corneal findings in two patients with arthrogryposis and discuss the implications for disease pathogenesis. Previous ophthalmologic reports are also reviewed.

Original languageEnglish
Pages (from-to)127-132
Number of pages6
JournalAustralian and New Zealand Journal of Ophthalmology
Volume22
Issue number2
DOIs
Publication statusPublished - 1 Jan 1994
Externally publishedYes

Fingerprint Dive into the research topics of 'Arthrogryposis multiplex congenita: A report of two cases'. Together they form a unique fingerprint.

Cite this