OSTEOGENESIS IMPERFECT A (CASE REPORT)

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HASHEMI S.B.; KABOODKHANI R.

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Journal Paper

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Journal: Armaghane Danesh Year:2005 | Volume:10 | Issue:4 (40) Page(s): 101-106

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Information Journal Paper

Title

OSTEOGENESIS IMPERFECT A (CASE REPORT)

Author(s)

HASHEMI S.B. | KABOODKHANI R. | Issue Writer Certificate

Keywords

OSTEOGENESIS IMPERFECTAQ4

OTOSCLEROSISQ3

STAPEDECTOMYQ3

TEFLON PISTONQ4

Abstract

Introduction & Objective: OSTEOGENESIS IMPERFECTA (OI) is a generalized connective tissue disorder and it is mostly inherited as an autosomal dominant trait. It may present with fragile bones, blue sclerae and hearing loss. We present two cases of OI. Case presentation: First case is a 18 Y/O man referred with bilateral hearing loss, who had 40db hearing loss in left side (operated ear) and underwent stapedotomy and received a good hearing. Second case is a 13 Y/O boy referred with bilateral hearing loss, who had 45db hearing loss in left side (operated ear) and underwent stapedotomy and received a good hearing with SRT less than 15. Conclusion: If the patient is selected properly, good result is achieved.

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APA: Copy

HASHEMI, S.B., & KABOODKHANI, R.. (2005). OSTEOGENESIS IMPERFECT A (CASE REPORT). ARMAGHAN DANESH, 10(4 (40)), 101-106. SID. https://sid.ir/paper/381189/en

Vancouver: Copy

HASHEMI S.B., KABOODKHANI R.. OSTEOGENESIS IMPERFECT A (CASE REPORT). ARMAGHAN DANESH[Internet]. 2005;10(4 (40)):101-106. Available from: https://sid.ir/paper/381189/en

IEEE: Copy

S.B. HASHEMI, and R. KABOODKHANI, “OSTEOGENESIS IMPERFECT A (CASE REPORT),” ARMAGHAN DANESH, vol. 10, no. 4 (40), pp. 101–106, 2005, [Online]. Available: https://sid.ir/paper/381189/en

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