AN IRREGULAR, FAMILIAL CHONDRO-OSSEOUS DEFECT

Author:

Jackson W. P.U.1

Affiliation:

1. The Department of Clinical Medicine, University of Cape Town, Cape Town, South Africa

Abstract

Three elderly sibling dwarfs are reported from a large and otherwise normal family. Their condition is an unusual and irregular form of cartilaginous defect, combined with club-feet, and bearing some resemblance to the Morquio type. A brief consideration of the literature of the generahised developmental bony syndromes shows confusion of thought and nomenclature. A plea is therefore made for simplification and a rational and simple grouping of these conditions is attempted. It seems particularly desirable that many confusing names for particular syndromes should be scrapped (for example, dyschondroplasia, chondro-osteodystrophy), although quite evidently the terms achondroplasia and osteogenesis imperfecta must remain because of their long-standing and general usage. Incidentally I have suggested elsewhere (Jackson 1951) that the name cleido-cranial dysostosis should be dropped, because it tends to lead the investigator away from the clinically more important lesions in the teeth and the cartilage bones of the pelvis and legs. It seems reasonable to confine the nomenclature of these various syndromes to the names used in the above classification, or something on those lines.

Publisher

British Editorial Society of Bone & Joint Surgery

Subject

Orthopedics and Sports Medicine,Surgery

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Der diastrophische Zwergwuchs;Zeitschrift für Orthopädie und ihre Grenzgebiete;2008-03-18

2. The phenotypic variability of diastrophic dysplasia;The Journal of Pediatrics;1978-10

3. DIASTROPHIC DWARFISM;Medicine;1972-01

4. EPIPHYSEAL DYSOSTOSIS;American Journal of Roentgenology;1969-04

5. Diastrophic dwarfism.;Archives of Disease in Childhood;1969-02-01

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