"Osteopetrosis" in the Fairbank Collection.

Abstract

The "osteopetrosis" section of the Fairbank Collection in the Radiology Museum of the Royal National Orthopaedic Hospital contains radiographs and case notes of twenty-two patients. This material has been reviewed in terms of modern concepts in an attempt to obtain a long-term follow-up and a firm diagnosis in each individual. Nine patients proved to have the classical autosomal dominant form of osteopetrosis, four had the malignant autosomal recessive type, craniometaphyseal dysplasia was present in two kindreds and isolated individuals had pyknodysostosis, atypical craniodiaphyseal dysplasia and craniosclerosis with osteopathia striata. As these conditions differ greatly in their clinical and genetic prognoses, diagnostic categorisation is of practical importance.

• Authors: F T Horan, P H Beighton
• Journal: The Journal of bone and joint surgery. British volume (J Bone Joint Surg Br) Vol. 60 Issue 1 Pg. 53-5 (Feb 1978) ISSN: 0301-620X [Print] England
• PMID: 342533 (Publication Type: Biography, Historical Article, Journal Article)

Topics

• Adolescent
• Adult
• Body Height
• Child
• Child, Preschool
• Facial Bones (diagnostic imaging)
• Female
• Follow-Up Studies
• Genes, Dominant
• History of Medicine
• History, Ancient
• Humans
• Infant
• London
• Male
• Museums
• Osteopetrosis (complications, diagnostic imaging, genetics, history)
• Radiography
• Skull (diagnostic imaging)