Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families.

Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. Research Abstract Details 

Research Abstract Table of Contents

Jump to the:

Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. Abstract Text:

C Dawe,R Wynne-Davies,G E Fulford,

Thirteen patients with dyschondrosteosis from eight families are reviewed and their clinical and radiographic variation noted. Inheritance is likely to be autosomal dominant but with only 50 per cent penetrance. Stature was moderately reduced, due to shortening of the bones of the leg. Radio-ulnar shortening could either involve both bones equally or the radius predominantly, in which case a typical Madelung deformity was seen. Tibio-fibular disproportion was present in half the patients, two of them having severe deformity associated with tibia varum and a long fibula. The treatment of one of these patients is described. It is recommended that patients with dyschondrosteosis should be kept under surveillance during the growing period. Problems in the limbs, especially the legs, may require operations to equalise the length of the two bones.

Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. Publishing Authors By Initials

C Dawe,R Wynne-Davies,GE Fulford,

For similar investigative techniques: genetic techniques: pedigree research abstracts see: investigative techniques: genetic techniques: pedigree research

PUBMED ID PMID:

MEDLINE DATE:

Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. Journal Published:

PUBLICATION TYPE: Journal Article

Journal: The Journal of bone and joint surgery. British vol

VOLUME: 64

Page Numbers: 377-81

Journal Abbreviation:

ISSN: 0301-620X

DAY: 14

MONTH: 02

YEAR: 1982

Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. Information

Number of References:

LANGUAGE: eng

NlmUniqueID: 375355

Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. Keywords Mesh Terms:

KEYWORDS: Pedigree

MESH TERMS: surgery

Chemical & Substance for Abstract: Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families. Information

Substance Name:

Registry Number:

Grant and Affiliation Information for Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families.

AFFILIATION:

Country: ENGLAND

AGENCY:

GRANT:

ACRONYM:

MEDLINETA: J Bone Joint Surg Br

REFSOURCE:

DATABASENAME:

ACCESSION NUMBER:

Number Hits: 0

Clinical variation in dyschondrosteosis A report on 13 individuals in 8 families Related Publications

• An aircraft accident: how to survive. Symposium at the Institution of Mechanical Engineers, London. January 8, 1991.
• Art--or science?
• Assessment of the Denham knee replacement. Results after eight years.
• Casualty trolley.
• Clinical variation in dyschondrosteosis. A report on 13 individuals in 8 families.
• Development of the treatment attitudes questionnaire in bipolar disorder.
• Electronic publishing--the next steps.
• Evaluative delusions: their significance for philosophy and psychiatry.
• Fraudulent and redundant publication.
• Lateral release for chondromalacia patellae.
• Muscle [phosphocreatine] dynamics following the onset of exercise in humans: the influence of baseline work-rate.
• Regulation of nociceptin/orphaninFQ secretion by immune cells and functional modulation of interleukin-2.
• Reply.
• Sterilisation of canine anterior cruciate allografts by gamma irradiation in argon. Mechanical and neurohistological properties retained one year after transplantation.
• Stress fracture of the radius.
• Subtalar arthrodesis by cancellous grafts and metallic internal fixation.
• Terrorism trials in the new century--how have things changed since the IRA trials?
• The prevention of tetanus.
• Trauma and orthopaedic surgeons.