Article citationsMore>>

Carey, M.C., Fitzgerald, O. and McKiernan, E. (1968) Osteogenesis Imperfecta in Twenty Three Members of a Kindred with Heritable Features Contributed by a Non-Specific Skeletal Disorder. Quarterly Journal of Medicine, 37, 437-449.

has been cited by the following article:

• TITLE: Carotid Artery Prolapse and Myringocarotidopexy in Osteogenesis Imperfecta

  AUTHORS: Hassanin Abdulkarim, Hassan Haidar, Ahmad Abualsoud, Ahmed Elsotouhy, A. Salam Alqahtani

  KEYWORDS: Eustachian Tube, Carotid Artery, Osteogenesis Imperfecta, Chronic Otitis Media, Myringocarotidopexy, Hearing Loss

  JOURNAL NAME: International Journal of Otolaryngology and Head & Neck Surgery, Vol.4 No.4, July 15, 2015

  ABSTRACT: Osteogenesis Imperfecta is a rare genetic disorder of connective tissue that is caused by an error in collagen formation. The disease is characterized by abnormal bone fragility, osteopenia, blue discoloration of the sclerae and hearing loss. Chronic non-suppurative otitis media is frequent in Osteogenesis Imperfecta patients and usually attributed to Eustachian tube dysfunction due to cranial molding and deformities. In some cases of severe Osteogenesis Imperfecta, the fragile bone of the petrous carotid canal can be broken down by the pulsations of the carotid artery, this may result in prolapse of the carotid artery into the protympanum with resultant Eustachian tube obstruction and tympanic membrane retraction with adhesion to prolapsed carotid artery, a condition called myringocarotidopexy.