Affiliation:
1. University Department of Surgery, Glasgow Royal Infirmary
Abstract
Abstract
A case of craniocleidal dysostosis was presented. In spite of the skeletal abnormalities present, the disease was not diagnosed until the patient, a married woman of 63, developed ischaemia of her right upper limb, followed by cerebral symptoms. An arch aortogram demonstrated an occlusion of the first part of the right subclavian artery involving the origin of the vertebral artery and a post-stenotic dilatation of the left subclavian artery due to costoclavicular compression. Such vascular abnormalities have not been previously described in this condition.
Publisher
Oxford University Press (OUP)
Reference11 articles.
1. Cleidocranial dysostosis;Abram;Lancet,1907
2. Deafness and cranio-cleido-dysostosis;Davis;Arch. Otolaryngol.,1954
3. Cleido-cranial dysostosis: hereditary and familial;Fitchet;J. Bone Joint Surg.,1929
4. Cleido-cranial dysostosis;Forland;Am. J. Med.,1962
5. Qsteo-dental dysplasia (cleido-cranial dysostosis);Jackson;Acta Med. Scand.,1950
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