مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

108
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

76
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

Hereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study

Pages

  10323-10334

Abstract

 Background: Our research focuses on different dimensions of families of Turkmen population of Iran with two or more than two affected members. A complete clinical ear test was conducted on them. It was aimed to find families with the highest chance of Hereditary hearing impairment among siblings and also existence of Consanguinity among their parents. Materials and Methods All Turkmen families with at least two hearing impaired members were screened based on prenatal and postnatal histories, family medical history, socioeconomic status as well as physical examination. For confirmation of hereditary hearing loss, a comprehensive evaluation including prenatal, perinatal and postnatal history, family medical history, pattern of inheritance, Consanguinity, and three generation pedigree, the physical examination, and genetic screening by a genetic expert were used. They were referred for complete hearing evaluation including pure tone audiometry, speech recognition threshold, otoacoustic emission and auditory brainstem response. Results A total of 82 families with 198 hearing impaired patients were diagnosed with about 60% having two and the rest with more than two affected members. Nearly 89% (n=175) of the patients had the inherited type of hearing loss among which 95% (n=167) demonstrated non-syndromic symptoms. The rate of Consanguinity among parents of the patients was about 65%. Conclusion This research revealed a high incidence of Hereditary hearing impairment and Consanguinity among Turkmen population which is in agreement with other reports from Iranian population with deaf children. In general, the rate of Consanguinity in Iranian population is 38%. Therefore, it seems that Consanguinity is higher in families with hearing-impaired children.

Cites

  • No record.

    • References

    Cite

    APA: Copy

    Hajilari, Maryam, OLADNABI, MORTEZA, KIANMEHR, ANVARSADAT, TAZIKI, MOHAMMAD HOSSEIN, & ZAMIRI ABDOLLAHI, FARZANEH. (2019). Hereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study. INTERNATIONAL JOURNAL OF PEDIATRICS, 7(11 (71)), 10323-10334. SID. https://sid.ir/paper/771751/en

    Vancouver: Copy

    Hajilari Maryam, OLADNABI MORTEZA, KIANMEHR ANVARSADAT, TAZIKI MOHAMMAD HOSSEIN, ZAMIRI ABDOLLAHI FARZANEH. Hereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study. INTERNATIONAL JOURNAL OF PEDIATRICS[Internet]. 2019;7(11 (71)):10323-10334. Available from: https://sid.ir/paper/771751/en

    IEEE: Copy

    Maryam Hajilari, MORTEZA OLADNABI, ANVARSADAT KIANMEHR, MOHAMMAD HOSSEIN TAZIKI, and FARZANEH ZAMIRI ABDOLLAHI, “Hereditary Hearing Loss and Consanguinity in Turkmen Population of Iran: A Retrospective Study,” INTERNATIONAL JOURNAL OF PEDIATRICS, vol. 7, no. 11 (71), pp. 10323–10334, 2019, [Online]. Available: https://sid.ir/paper/771751/en

    Related Journal Papers

  • No record.

    • Related Seminar Papers

  • No record.

    • Related Plans

  • No record.

    • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button