Dergiler / Turkish Journal of Medical Sciences / 2016 / Cilt: 46 - Sayı: 1

Ophthalmic pathologies in female subjects with bilateralcongenital sensorineural hearing loss

Sayfa
139–144
Yayın Tarihi
2022-11-05
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The high rate of visually debilitating syndromic ocular pathologies associated with high frequency of consanguinity doubles the importance.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:Background/aim: The high prevalence of ophthalmologic pathologies in hearing-disabled subjects necessitates early screening of other sensory deficits, especially visual function.
📊
Temel Bulgular & Veri:Materials and methods: This descriptive study is a prospective analysis of 78 young female SNHL subjects who were examined at a tertiary care university hospital with a detailed ophthalmic examination, including electroretinography (ERG) and visual field tests as needed.
💡
Sonuç & Katkı:The high rate of visually debilitating syndromic ocular pathologies associated with high frequency of consanguinity doubles the importance.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Alan Parametreleri

Abstract

Background/aim: The high prevalence of ophthalmologic pathologies in hearing-disabled subjects necessitates early screening of other sensory deficits, especially visual function. The aim of this study is to determine the frequency and clinical characteristics of ophthalmic pathologies in patients with congenital bilateral sensorineural hearing loss (SNHL). Materials and methods: This descriptive study is a prospective analysis of 78 young female SNHL subjects who were examined at a tertiary care university hospital with a detailed ophthalmic examination, including electroretinography (ERG) and visual field tests as needed. Results: The mean age was 19.00 ± 1.69 years (range: 15 to 24 years). A total of 39 cases (50%) had at least one ocular pathology. Refractive errors were the leading problem, found in 35 patients (44.9%). Anterior segment examination revealed heterochromia iridis or Waardenburg syndrome in 2 cases (2.56%). Dilated fundus examination revealed retinal pathologies in 15 cases (19.23%), including retinitis pigmentosa or Usher s syndrome in 8 cases (10.25%). Most of the Usher s syndrome cases (87.5%) had consanguinity. Conclusion: Screening for congenital SNHL in the early years of life and routine yearly follow-ups are essential for maximizing the rehabilitation of this disabled group. The high rate of visually debilitating syndromic ocular pathologies associated with high frequency of consanguinity doubles the importance.

🔖

Bu Makaleye Atıf Yap

GÖKÇE, G., AKINCIOĞLU, D., KÖYLÜ, M. T., OYSUL, F. G., SOBACI, G. (2022). Ophthalmic pathologies in female subjects with bilateralcongenital sensorineural hearing loss. Turkish Journal of Medical Sciences, Cilt: 46 - Sayı: 1, 139–144. https://ajindex.com/articles/610722

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (17)

  1. Smith RJ, Bale JF Jr, White KR. Sensorineural hearing loss in children. Lancet 2005; 365: 879–890
  2. Cummings CW, Flint PW, Phelps T, Abuzeid WM. Cummings Otolaryngology: Head & Neck Surgery. Philadelphia, PA, USA: Elsevier Mosby; 2005
  3. Chan KH. Sensorineural hearing loss in children. Classification and evaluation. Otolaryngol Clin North Am 1994; 27: 473–486
  4. Mafong DD, Pletcher SD, Hoyt C, Lalwani AK. Ocular findings in children with congenital sensorineural hearing loss. Arch Otolaryngol Head Neck Surg 2002; 128: 1303–1306
  5. Bess FH, Paradise JL. Universal screening for infant hearing impairment: not simple, not risk-free, not necessarily beneficial, and not presently justified. Pediatrics 1994; 93: 330– 334
  6. Fillman RD, Leguire L, Rogers GL, Bremer DL, Fellows RR. Screening for vision problems, including Usher syndrome, among hearing impaired students. Am Ann Deaf 1987; 132: 194–198
  7. Bakhshaee M, Banaee T, Ghasemi MM, Nourizadeh N, Shojaee B, Shahriari S. Ophthalmic disturbances in children with sensorineural hearing loss. Eur Arch Otorhinolaryngol 2009; 266: 823–825
  8. Regenbogen L, Godel V. Ocular deficiencies in deaf children. J Pediatr Ophthalmol Strabismus 1984; 22: 231–233
  9. Guy R, Nicholson J, Pannu S, Holden R. A clinical evaluation of ophthalmic assessment in children with sensori‐neural deafness. Child Care Health Dev 2003; 29: 377–384
  10. Armitage I, Burke J, Buffin J. Visual impairment in severe and profound sensorineural deafness. Arch Dis Child 1995; 73: 53–56
  11. Ceyhan D, Aysun İ, Özdemir O, Calıskan D. Ophthalmologic screening in a school for the hearing impaired in Turkey. Turk Clin J Med Sci 2011; 31: 1484–1490
  12. Suchman RG. Visual impairment among deaf children: frequency and educational consequences. Arch Ophthalmol 1967; 77: 18
  13. Mets MB, Young NM, Pass A, Lasky JB. Early diagnosis of Usher syndrome in children. Trans Am Ophthalmol Soc 2000; 98: 237–245
  14. Marmor M, Fulton A, Holder G, Miyake Y, Brigell M, Bach M. ISCEV Standard for full-field clinical electroretinography (2008 update). Doc Ophthalmol 2009; 118: 69–77
  15. Hamel C. Retinitis pigmentosa. Orphanet J Rare Dis 2006; 1: 40
  16. Hanioğlu-Kargı S, Köksal M, Tomaç S, Uğurbaş SH, Alpay A. Ophthalmologic abnormalities in children from a Turkish school for the deaf. Turk J Pediatr 2003; 45: 39–42
  17. Brinks MV, Murphey WH, Cardwell W, Otos M, Weleber RG. Ophthalmologic screening of deaf students in Oregon. J Pediatr Ophthalmol Strabismus 2000;