Literature DB >> 29761033

Diagnosis and Treatment of Congenital Sensorineural Hearing Loss.

Divya A Chari1, Dylan K Chan1.   

Abstract

PURPOSE OF REVIEW: The aim of this report is to review current literature regarding the work-up and management of congenital sensorineural hearing loss. RECENT
FINDINGS: Diagnostic evaluation of a newborn with sensorineural hearing loss begins with a complete audiologic evaluation and comprehensive history and physical exam. This review presents a diagnostic algorithm for the work-up of congenital hearing loss, focusing on the three following modalities: cytomegalovirus testing, genetic evaluation, and imaging.
SUMMARY: Newborn hearing loss is a common problem and may be attributed to genetic and non-genetic factors. Complete diagnostic evaluation and treatment are essential for preventing delays in language development. Treatment consists of early intervention services and consideration of hearing aid amplification and cochlear implantation.

Entities:  

Keywords:  Congenital hearing loss; cochlear implantation; cytomegalovirus; diagnosis; newborn hearing screen; prelingual deafness

Year:  2017        PMID: 29761033      PMCID: PMC5947965          DOI: 10.1007/s40136-017-0163-3

Source DB:  PubMed          Journal:  Curr Otorhinolaryngol Rep


  38 in total

1.  Genome-wide SNP genotyping identifies the Stereocilin (STRC) gene as a major contributor to pediatric bilateral sensorineural hearing impairment.

Authors:  Lauren J Francey; Laura K Conlin; Hanna E Kadesch; Dinah Clark; Donna Berrodin; Yi Sun; Joe Glessner; Hakon Hakonarson; Chaim Jalas; Chaim Landau; Nancy B Spinner; Margaret Kenna; Michal Sagi; Heidi L Rehm; Ian D Krantz
Journal:  Am J Med Genet A       Date:  2011-12-06       Impact factor: 2.802

2.  Early acquisition of cytomegalovirus infection.

Authors:  C S Peckham; C Johnson; A Ades; K Pearl; K S Chin
Journal:  Arch Dis Child       Date:  1987-08       Impact factor: 3.791

3.  The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands.

Authors:  Celia Zazo Seco; Mieke Wesdorp; Ilse Feenstra; Rolph Pfundt; Jayne Y Hehir-Kwa; Stefan H Lelieveld; Steven Castelein; Christian Gilissen; Ilse J de Wijs; Ronald Jc Admiraal; Ronald Je Pennings; Henricus Pm Kunst; Jiddeke M van de Kamp; Saskia Tamminga; Arjan C Houweling; Astrid S Plomp; Saskia M Maas; Pia Am de Koning Gans; Sarina G Kant; Christa M de Geus; Suzanna Gm Frints; Els K Vanhoutte; Marieke F van Dooren; Marie-José H van den Boogaard; Hans Scheffer; Marcel Nelen; Hannie Kremer; Lies Hoefsloot; Margit Schraders; Helger G Yntema
Journal:  Eur J Hum Genet       Date:  2016-12-21       Impact factor: 4.246

Review 4.  Diagnostic yield of computed tomography scan for pediatric hearing loss: a systematic review.

Authors:  Jenny X Chen; Bart Kachniarz; Jennifer J Shin
Journal:  Otolaryngol Head Neck Surg       Date:  2014-09-03       Impact factor: 3.497

5.  Cognitive and behavioral outcomes after early exposure to anesthesia and surgery.

Authors:  Randall P Flick; Slavica K Katusic; Robert C Colligan; Robert T Wilder; Robert G Voigt; Michael D Olson; Juraj Sprung; Amy L Weaver; Darrell R Schroeder; David O Warner
Journal:  Pediatrics       Date:  2011-10-03       Impact factor: 7.124

6.  Long-term follow-up of hearing loss in children and young adults with enlarged vestibular aqueducts: relationship to radiologic findings and Pendred syndrome diagnosis.

Authors:  Ian B Colvin; Timothy Beale; Katherine Harrop-Griffiths
Journal:  Laryngoscope       Date:  2006-11       Impact factor: 3.325

7.  Middle ear effusions in neonates.

Authors:  T J Balkany; S A Berman; M A Simmons; B W Jafek
Journal:  Laryngoscope       Date:  1978-03       Impact factor: 3.325

8.  Language ability after early detection of permanent childhood hearing impairment.

Authors:  Colin R Kennedy; Donna C McCann; Michael J Campbell; Catherine M Law; Mark Mullee; Stavros Petrou; Peter Watkin; Sarah Worsfold; Ho Ming Yuen; Jim Stevenson
Journal:  N Engl J Med       Date:  2006-05-18       Impact factor: 91.245

9.  Comprehensive genetic testing in the clinical evaluation of 1119 patients with hearing loss.

Authors:  Christina M Sloan-Heggen; Amanda O Bierer; A Eliot Shearer; Diana L Kolbe; Carla J Nishimura; Kathy L Frees; Sean S Ephraim; Seiji B Shibata; Kevin T Booth; Colleen A Campbell; Paul T Ranum; Amy E Weaver; E Ann Black-Ziegelbein; Donghong Wang; Hela Azaiez; Richard J H Smith
Journal:  Hum Genet       Date:  2016-03-11       Impact factor: 4.132

10.  Screening for seemingly healthy newborns with congenital cytomegalovirus infection by quantitative real-time polymerase chain reaction using newborn urine: an observational study.

Authors:  Akira Yamaguchi; Tsutomu Oh-Ishi; Takashi Arai; Hideaki Sakata; Nodoka Adachi; Satoshi Asanuma; Eiji Oguma; Hirofumi Kimoto; Jiro Matsumoto; Hidetoshi Fujita; Tadashi Uesato; Jutaro Fujita; Ken Shirato; Hideki Ohno; Takako Kizaki
Journal:  BMJ Open       Date:  2017-01-20       Impact factor: 2.692

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  3 in total

1.  A novel variant in DMXL2 gene is associated with autosomal dominant non-syndromic hearing impairment (DFNA71) in a Cameroonian family.

Authors:  Edmond Wonkam-Tingang; Isabelle Schrauwen; Kevin K Esoh; Thashi Bharadwaj; Liz M Nouel-Saied; Anushree Acharya; Abdul Nasir; Suzanne M Leal; Ambroise Wonkam
Journal:  Exp Biol Med (Maywood)       Date:  2021-03-09

2.  Assessing Cerebral White Matter Microstructure in Children With Congenital Sensorineural Hearing Loss: A Tract-Based Spatial Statistics Study.

Authors:  Muliang Jiang; Zuguang Wen; Liling Long; Chi Wah Wong; Ningrong Ye; Chishing Zee; Bihong T Chen
Journal:  Front Neurosci       Date:  2019-06-21       Impact factor: 4.677

3.  Outcomes of Gene Panel Testing for Sensorineural Hearing Loss in a Diverse Patient Cohort.

Authors:  Elizabeth N Liao; Emily Taketa; Noura I Mohamad; Dylan K Chan
Journal:  JAMA Netw Open       Date:  2022-09-01
  3 in total

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