CHARGE syndrome: A window of opportunity for audiologic intervention

Pediatrics

Volumn 110, Issue 1 I, 2002, Pages 119-126

  Edwards, Bruce M ^a   Kileny, Paul R ^a   Van Riper, Lori A ^a  

^a UNIVERSITY OF MICHIGAN HEALTH SYSTEM   (United States)

Author keywords

Audiologic intervention; Auditory brainstem response; Behavioral hearing tests; CHARGE syndrome; Congenital facial palsy; Multiple congenital anomalies

Indexed keywords

ARTICLE; AUDIOLOGY; AUDITORY RESPONSE; BRAIN STEM RESPONSE; CHILD; CHILD DEVELOPMENT; CHOANA ATRESIA; CLINICAL ARTICLE; COLOBOMA; CONGENITAL HEART MALFORMATION; DISEASE ASSOCIATION; EAR MALFORMATION; EARLY DIAGNOSIS; FACIAL NERVE PARALYSIS; FEMALE; GENITAL MALFORMATION; HEARING LOSS; HEARING TEST; HUMAN; HYPOPLASIA; INFANT; MALE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SYNDROME CHARGE;

ABNORMALITIES, MULTIPLE; AGE FACTORS; CHILD, PRESCHOOL; DEVELOPMENTAL DISABILITIES; EVOKED POTENTIALS, AUDITORY, BRAIN STEM; FACIAL PARALYSIS; FEMALE; HEARING AIDS; HEARING LOSS, SENSORINEURAL; HEARING TESTS; HUMANS; INFANT; INFANT, NEWBORN; MALE; NEONATAL SCREENING; SYNDROME;

EID: 0036302843     PISSN: 00314005     EISSN: None     Source Type: Journal    
DOI: 10.1542/peds.110.1.119     Document Type: Article

References (53)

1. Choanal atresia and associated multiple anomalies
2. Colobomatous microphthalmia, heart disease, hearing loss, and mental retardation-a syndrome
3. Coloboma, congenital heart disease, and choanal atresia with multiple anomalies: CHARGE association
4. CHARGE syndrome: Report of 47 cases and review
5. Pathological features of the CHARGE association: Support for involvement of the neural crest
6. Choanal atresia and its associated anomalies. Further support for the CHARGE association
7. Clinical manifestations of CHARGE association
8. Apparent CHARGE association and chromosome anomaly: Chance or contiguous gene syndrome?
9. Balanced t(6;8)(6p8p6q8q) and the CHARGE association
10. CHARGE association in a child with de novo inverted duplication (14)(q22 >q24.3)
11. CHARGE association-related ocular pathology in a newborn with partial trisomy 19q and partial monosomy 21q, from a maternal translocation (19;21)(q13.1; q22.3)
12. Familial CHARGE syndrome: Clinical report with autopsy findings
13. CHARGE association anomalies in siblings
14. Dominant CHARGE association
15. Increased paternal age in CHARGE association
16. Properties of associations: Identity, nature, and clinical criteria, with a commentary on why CHARGE and Goldenhar are not associations
17. CHARGE association: Report of 47 cases with genotypic analysis of chromosomes 7q36 and 22q11
18. Mutation of PAX2 in two siblings with renal-coloboma syndrome
19. Mutation of the PAX2 gene in a family with optic nerve colobomas, renal anomalies, and vesicoureteral reflux
20. Expression of the PAX2 gene in human embryos and exclusion in the CHARGE syndrome
21. Ocular colobomata and multiple congenital anomalies: The CHARGE association
22. Diagnosis, genetics and prenatal diagnosis in CHARGE
23. Earnose-throat abnormalities in the CHARGE association
24. Vestibular anomalies in CHARGE association
25. CT of the temporal bone in the CHARGE association
26. Otological manifestations of CHARGE association
27. Vestibular function in children with the CHARGE association
28. Vestibular anomalies in CHARGE syndrome
29. CHARGE association: An update and review for the primary pediatrician
30. Audiologic and educational issues in CHARGE syndrome
31. The eye in CHARGE association
32. Ocular findings in CHARGE syndrome. Six case reports and a review
33. CHARGE association with congenital glaucoma due to maldevelopment of the anterior chamber angle
34. CHARGE syndrome: Part II. Hearing loss
35. Otologic management in children with the CHARGE association
36. The CHARGE association: Implications for teachers
37. Survey on management of hearing loss in CHARGE syndrome
38. The frequency specificity of tone-pip evoked auditory brain stem responses
39. Predictive value of ABR in infants and children with moderate to profound hearing impairment
40. Audiology clinical practice algorithms and statements
41. Newborn and infant hearing loss: Detection and intervention
42. Guidelines for screening for hearing impairment: Neonates and young infants, birth through 6 months
43. Joint Committee on Infant Hearing
44. Early identification of congenital sensorineural hearing impairment
45. On the real age of identification of congenital hearing loss
46. Age of suspicion, identification, and intervention for infants and young children with hearing loss: A national study
47. The New York State universal newborn hearing screening demonstration project: Ages of hearing loss identification, hearing aid fitting, and enrollment in early intervention
48. Cranial nerve abnormalities in CHARGE Association
49. Language of early and later-identified children with hearing loss
50. Audiologic findings in a set of fraternal twins with CHARGE association
51. CHARGE association