Severe to profound hearing loss in patients with progressed Alport's syndrome

Acta Oto-Laryngologica

Volumn 129, Issue 9, 2009, Pages 982-987

  Moon, In Seok ^a   Bang, Mi Young ^b   Shim, Dae Bo ^b   Shin, Seung Ho ^b   Choi, Jae Young ^b  

^a Chung Ang University   (South Korea)

^b Yonsei University   (South Korea)

Author keywords

Alport's syndrome; Hearing loss; Otoacoustic emission

Indexed keywords

ADOLESCENT; ADULT; ALPORT SYNDROME; ARTICLE; AUDITORY THRESHOLD; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DISEASE COURSE; DISEASE DURATION; DISEASE SEVERITY; EVOKED OTOACOUSTIC EMISSION; FEMALE; HEARING LOSS; HUMAN; KIDNEY DISEASE; KIDNEY FAILURE; KIDNEY FUNCTION; LONGEVITY; MALE; OTOACOUSTIC EMISSION; PERCEPTION DEAFNESS; PRIORITY JOURNAL; PURE TONE AUDIOMETRY; RETROSPECTIVE STUDY; SCHOOL CHILD; SPEECH; SPEECH AUDIOMETRY;

ADOLESCENT; ADULT; AUDIOMETRY; CHILD; FEMALE; HEARING; HEARING LOSS, SENSORINEURAL; HUMANS; KIDNEY; MALE; NEPHRITIS, HEREDITARY; RETROSPECTIVE STUDIES; SEX FACTORS; YOUNG ADULT;

EID: 70350353197     PISSN: 00016489     EISSN: 16512553     Source Type: Journal    
DOI: 10.1080/00016480802545588     Document Type: Article

References (19)

1. Alport AC. Hereditary congenital hemorrhagic nephritis. BMJ 1927;/1:/504-6.
2. Kashtan CE. Alport syndrome: an inherited disorder of renal, ocular and cochlear basement membranes. Medicine (Baltimore) 1999;/78:/338-360.
3. Zehnder AF, Adams JC, Santi PA, Kristiansen AC, Wacharasindhu C, Mann S, et al. Distiribution of type IV collagen in cochlear in Alport syndrome. Arch Otolaryngol Head Neck Surg 2005;/131:/1007-1013.
4. Kleppel MM, Santi PA, Cameron JD, Wieslander J, Michael AF. Human tissue distribution of novel basement membrane collagen. Am J Pathol 1989;/134:/813-825.
5. Merchant SN, Burgess BJ, Kashtan CE, Gregory MC, Santi PA, Colvin R, et al. Temporal bone histopathology in Alport syndrome. Laryngoscope 2004;/114:/1609-1618.
6. Schuknecht HF. Pathology of the ear, 2nd edn. New York: Lea & Febiger; 1993.
7. Kashtan CE. Renal transplantation in patients with Alport syndrome. Pediatr Transplant 2006;/10:/651-657.
8. Alves FRA, Riberio FQA. Revision about hearing loss in the Alport's syndrome, analyzing the clinical, genetic, and biomolecular aspects. Rev Bras Otorrhinolaryngol 2005;/71:/ 813-819
9. Gleeson MJ, Hons BDS. Alport's syndrome: audiologic manifestations and implications. J Laryngol Otol 1984;/98:/ 449-465
10. Rintelmann W. Auditory manifestations of Alport's disease syndrome. Trans Acad Ophthalmol Otolaryngol 1976;/82:/ 375-387
11. Sirimanna KS, France E, Stephens SDG. Alport's syndrome: can carriers be identified by audiometry? Clin Otolaryngol 1995;/20:/158-163.
12. Wester DC, Atkin CL, Gregory MC. Alport syndrome: clinical update. J Am Acad Audiol 1995;/6:/73-79.
13. Gregory MC, Terreros DA, Barker DF, Fain PN, Denison JC, Atkin CL. Alport syndrome - clinical phenotypes, incidence, and pathology. Contrib Nephrol 1996;/117:/21-28.
14. Kim HY, Kim PK, Choi JW, Kim YS, Park K. The prognosis of renal transplantation in Alport syndrome. J Korean Soc Transplant 1996;/10:/123-130.
15. Yassin A, Bardy A, Fatt-hi A. The relationship between electrolyte balance and cochlear disturbances in cases of renal failure. J Laryngol 1970;/84:/429-434.
16. Johnson DW, Mathog RH. Hearing function and chronic renal failure. Ann Otol Rhinol Laryngol 1976;/85:/43-45.
17. Spencer JT. Hyperlipoproteinemia in the etiology of inner ear disease. Laryngoscope 1973;/83:/639-671.
18. McDonald TJ, Jincke H, Anderson CF, Ott NT. Reversal of deafness after renal transplantation in Alport's syndrome. Laryngoscope 1978;/88:/38-42.
19. Longo I, Scala E, Mari F, Caselli R, Chiara P, Mencarelli MA, et al. Autosomal recessive Alport syndrome; an indepth clinical and molecular analysis of five families. Nephrol Dial Transplant 2006;/21:/665-671.