Hearing Impairment Medication

1. Morton NE. Genetic epidemiology of hearing impairment. Ann N Y Acad Sci. 1991. 630:16-31. [QxMD MEDLINE Link].

2. Erenberg A, Lemons J, Sia C, Trunkel D, Ziring P. Newborn and infant hearing loss: detection and intervention. American Academy of Pediatrics. Task Force on Newborn and Infant Hearing, 1998- 1999. Pediatrics. 1999 Feb. 103 (2):527-30. [QxMD MEDLINE Link].

3. Johnson JL, White KR, Widen JE, Gravel JS, James M, Kennalley T, et al. A multicenter evaluation of how many infants with permanent hearing loss pass a two-stage otoacoustic emissions/automated auditory brainstem response newborn hearing screening protocol. Pediatrics. 2005 Sep. 116 (3):663-72. [QxMD MEDLINE Link].

4. Katbamna B, Crumpton T, Patel DR. Hearing impairment in children. Pediatr Clin North Am. 2008 Oct. 55 (5):1175-88, ix. [QxMD MEDLINE Link].

5. Kenna MA. Neonatal hearing screening. Pediatr Clin North Am. 2003 Apr. 50 (2):301-13. [QxMD MEDLINE Link].

6. Kerschner JE. Neonatal hearing screening: to do or not to do. Pediatr Clin North Am. 2004 Jun. 51 (3):725-36, x. [QxMD MEDLINE Link].

7. Berg AL, Spitzer JB, Towers HM, Bartosiewicz C, Diamond BE. Newborn hearing screening in the NICU: profile of failed auditory brainstem response/passed otoacoustic emission. Pediatrics. 2005 Oct. 116 (4):933-8. [QxMD MEDLINE Link].

8. Cohn ES, Kelley PM, Fowler TW, Gorga MP, Lefkowitz DM, Kuehn HJ, et al. Clinical studies of families with hearing loss attributable to mutations in the connexin 26 gene (GJB2/DFNB1). Pediatrics. 1999 Mar. 103 (3):546-50. [QxMD MEDLINE Link].

9. Joint Committee on Infant Hearing., American Academy of Audiology., American Academy of Pediatrics., American Speech-Language-Hearing Association., Directors of Speech and Hearing Programs in State Health and Welfare Agencies. Year 2000 position statement: principles and guidelines for early hearing detection and intervention programs. Joint Committee on Infant Hearing, American Academy of Audiology, American Academy of Pediatrics, American Speech-Language-Hearing Association, and Directors of Speech and Hearing Programs in State Health and Welfare Agencies. Pediatrics. 2000 Oct. 106 (4):798-817. [QxMD MEDLINE Link].

10. [Guideline] American Academy of Pediatrics, Joint Committee on Infant Hearing. Year 2007 position statement: Principles and guidelines for early hearing detection and intervention programs. Pediatrics. 2007 Oct. 120 (4):898-921. [QxMD MEDLINE Link].

11. [Guideline] US Preventive Services Task Force. Universal screening for hearing loss in newborns: US Preventive Services Task Force recommendation statement. Pediatrics. 2008 Jul. 122 (1):143-8. [QxMD MEDLINE Link].

12. Nelson HD, Bougatsos C, Nygren P, 2001 US Preventive Services Task Force. Universal newborn hearing screening: systematic review to update the 2001 US Preventive Services Task Force Recommendation. Pediatrics. 2008 Jul. 122 (1):e266-76. [QxMD MEDLINE Link].

13. Kennedy CR, McCann DC, Campbell MJ, Law CM, Mullee M, Petrou S, et al. Language ability after early detection of permanent childhood hearing impairment. N Engl J Med. 2006 May 18. 354 (20):2131-41. [QxMD MEDLINE Link].

14. [Guideline] Alford RL, Arnos KS, Fox M, et al, ACMG Working Group on Update of Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss, Professional Practice and Guidelines Committee. American College of Medical Genetics and Genomics guideline for the clinical evaluation and etiologic diagnosis of hearing loss. Genet Med. 2014 Apr. 16 (4):347-55. [QxMD MEDLINE Link].

15. Roizen NJ. Etiology of hearing loss in children. Nongenetic causes. Pediatr Clin North Am. 1999 Feb. 46 (1):49-64, x. [QxMD MEDLINE Link].

16. McGee J, Walsh EJ. Cochlear transduction and the molecular basis of auditory pathology. Flint PW, Francis HW, Haughey BH, Lesperance MM, Lund VJ, Robbins KT, et al, eds. Cummings Otolaryngology: Head & Neck Surgery. 7th ed. Philadelphia: Elsevier; 2021. 2221-68.

17. Shearer AE, Shibata SB, Smith RJH. Genetic sensorineural hearing loss. Flint PW, Francis HW, Haughey BH, Lesperance MM, Lund VJ, Robbins KT, et al, eds. Cummings Otolaryngology: Head & Neck Surgery. 7th ed. Philadelphia: Elsevier; 2021. 2279-92.

18. Marlin S, Garabédian EN, Roger G, Moatti L, Matha N, Lewin P, et al. Connexin 26 gene mutations in congenitally deaf children: pitfalls for genetic counseling. Arch Otolaryngol Head Neck Surg. 2001 Aug. 127 (8):927-33. [QxMD MEDLINE Link].

19. Tashiro K, Konishi H, Sano E, Nabeshi H, Yamauchi E, Taniguchi H. Suppression of the ligand-mediated down-regulation of epidermal growth factor receptor by Ymer, a novel tyrosine-phosphorylated and ubiquitinated protein. J Biol Chem. 2006 Aug 25. 281 (34):24612-22. [QxMD MEDLINE Link].

20. Modamio-Hoybjor S, Mencia A, Goodyear R, del Castillo I, Richardson G, Moreno F, et al. A mutation in CCDC50, a gene encoding an effector of epidermal growth factor-mediated cell signaling, causes progressive hearing loss. Am J Hum Genet. 2007 Jun. 80 (6):1076-89. [QxMD MEDLINE Link]. [Full Text].

21. Bondurand N, Pingault V, Goerich DE, Lemort N, Sock E, Le Caignec C, et al. Interaction among SOX10, PAX3 and MITF, three genes altered in Waardenburg syndrome. Hum Mol Genet. 2000 Aug 12. 9 (13):1907-17. [QxMD MEDLINE Link].

22. Richardson SO. The child with "delayed speech". Contemp Pediatr. 1992. 9(9):55.

23. Schieffer KM, Connor JR, Pawelczyk JA, Sekhar DL. The Relationship Between Iron Deficiency Anemia and Sensorineural Hearing Loss in the Pediatric and Adolescent Population. Am J Audiol. 2017 Jun 13. 26 (2):155-162. [QxMD MEDLINE Link].

24. Parodi M, Rouillon I, Rebours C, Denoyelle F, Loundon N. Childhood psychogenic hearing loss: Identification and diagnosis. Eur Ann Otorhinolaryngol Head Neck Dis. 2017 Dec. 134 (6):415-418. [QxMD MEDLINE Link].

25. Shargorodsky J, Curhan SG, Curhan GC, Eavey R. Change in prevalence of hearing loss in US adolescents. JAMA. 2010 Aug 18. 304 (7):772-8. [QxMD MEDLINE Link].

26. Harrison M, Roush J, Wallace J. Trends in age of identification and intervention in infants with hearing loss. Ear Hear. 2003 Feb. 24 (1):89-95. [QxMD MEDLINE Link].

27. Smith RJ, Hone S. Genetic screening for deafness. Pediatr Clin North Am. 2003 Apr. 50 (2):315-29. [QxMD MEDLINE Link].

28. ACMG. Genetics Evaluation Guidelines for the Etiologic Diagnosis of Congenital Hearing Loss. Genetic Evaluation of Congenital Hearing Loss Expert Panel. ACMG statement. Genet Med. 2002 May-Jun. 4 (3):162-71. [QxMD MEDLINE Link].

29. Choung YH, Moon SK, Park HJ. Functional study of GJB2 in hereditary hearing loss. Laryngoscope. 2002 Sep. 112 (9):1667-71. [QxMD MEDLINE Link].

30. Gasparini P, Rabionet R, Barbujani G, Melçhionda S, Petersen M, Brøndum-Nielsen K, et al. High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG. Eur J Hum Genet. 2000 Jan. 8 (1):19-23. [QxMD MEDLINE Link].

31. Green GE, Scott DA, McDonald JM, Woodworth GG, Sheffield VC, Smith RJ. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness. JAMA. 1999 Jun 16. 281 (23):2211-6. [QxMD MEDLINE Link].

32. Parry DA, Booth T, Roland PS. Advantages of magnetic resonance imaging over computed tomography in preoperative evaluation of pediatric cochlear implant candidates. Otol Neurotol. 2005 Sep. 26 (5):976-82. [QxMD MEDLINE Link].

33. Joint Committee on Infant Hearing of the American Academy of Pediatrics, Muse C, Harrison J, Yoshinaga-Itano C, et al. Supplement to the JCIH 2007 position statement: principles and guidelines for early intervention after confirmation that a child is deaf or hard of hearing. Pediatrics. 2013 Apr. 131 (4):e1324-49. [QxMD MEDLINE Link].

34. Berlin CI, Morlet T, Hood LJ. Auditory neuropathy/dyssynchrony: its diagnosis and management. Pediatr Clin North Am. 2003 Apr. 50 (2):331-40, vii-viii. [QxMD MEDLINE Link].

35. Brookhouser PE, Beauchaine KL, Osberger MJ. Management of the child with sensorineural hearing loss. Medical, surgical, hearing aids, cochlear implants. Pediatr Clin North Am. 1999 Feb. 46 (1):121-41. [QxMD MEDLINE Link].

36. Carter JM, Hoff SR. Endoscopic middle ear exploration in pediatric patients with conductive hearing loss. Int J Pediatr Otorhinolaryngol. 2017 May. 96:21-24. [QxMD MEDLINE Link].

37. Cunningham M, Thomson V, McKiever E, Dickinson LM, Furniss A, Allison MA. Infant, Maternal, and Hospital Factors' Role in Loss to Follow-up After Failed Newborn Hearing Screening. Acad Pediatr. 2018 Mar. 18 (2):188-195. [QxMD MEDLINE Link].

Rahul K Shah, MD, FACS, FAAP Associate Professor of Otolaryngology and Pediatrics, Associate Surgeon-in-Chief, Medical Director, Peri-operative Services, Children's National Medical Center, George Washington University School of Medicine and Health Sciences; Attending Physician, Department of Otolaryngology, Children's National Medical Center

Rahul K Shah, MD, FACS, FAAP is a member of the following medical societies: Alpha Omega Alpha, American Academy of Otolaryngology-Head and Neck Surgery, American Academy of Pediatrics, American College of Medical Quality, American Association for Physician Leadership, American College of Surgeons, Triological Society, Massachusetts Medical Society, Phi Beta Kappa

Disclosure: Nothing to disclose.

Michael Lotke, MD Pediatric Clinical Educator, Mount Sinai Hospital–Chicago/Sinai Children’s Hospital; Assistant Professor, Department of Pediatrics, Rosalind Franklin University of Medicine and Science

Michael Lotke, MD is a member of the following medical societies: American Academy of Pediatrics, American Public Health Association

Disclosure: Nothing to disclose.

Mary L Windle, PharmD Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

John E McClay, MD, FAAP Associate Professor of Pediatric Otolaryngology, Department of Otolaryngology-Head and Neck Surgery, Children's Hospital of Dallas, University of Texas Southwestern Medical Center

John E McClay, MD, FAAP is a member of the following medical societies: American Academy of Otolaryngic Allergy, American Academy of Otolaryngology-Head and Neck Surgery, American College of Surgeons, American Medical Association

Disclosure: Nothing to disclose.

Ravindhra G Elluru, MD, PhD Professor, Wright State University, Boonshoft School of Medicine; Pediatric Otolaryngologist, Department of Otolaryngology, Dayton Children's Hospital Medical Center

Ravindhra G Elluru, MD, PhD is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery, American Academy of Pediatrics, American Bronchoesophagological Association, American College of Surgeons, American Medical Association, Association for Research in Otolaryngology, Society for Ear, Nose and Throat Advances in Children, Triological Society, American Society for Cell Biology

Disclosure: Nothing to disclose.

Orval Brown, MD Director of Otolaryngology Clinic, Professor, Department of Otolaryngology-Head and Neck Surgery, University of Texas Southwestern Medical Center at Dallas

Orval Brown, MD is a member of the following medical societies: American Academy of Otolaryngology-Head and Neck Surgery, American Academy of Pediatrics, American Bronchoesophagological Association, American College of Surgeons, American Medical Association, American Society of Pediatric Otolaryngology, Society for Ear, Nose and Throat Advances in Children, and Society of University Otolaryngologists-Head and Neck Surgeons

Disclosure: Nothing to disclose.

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