Successful cochlear implantation in a child with Keratosis, Icthiosis and Deafness (KID) Syndrome and Dandy-Walker malformation

International Journal of Pediatric Otorhinolaryngology

Volumn 72, Issue 5, 2008, Pages 693-698

  Cushing, Sharon L ^a   MacDonald, Laurie ^a   Propst, Evan J ^a   Sharma, Alok ^a   Stockley, Tracy ^a   Blaser, Susan L ^a   James, Adrian L ^a   Papsin, Blake C ^a  

^a HOSPITAL FOR SICK CHILDREN   (Canada)

Author keywords

Cerebellum; Cochlear implant; Connexin 26; Dandy Walker malformation; Genetics; GJB2; KID Syndrome; Pediatrics; Sensorineural hearing loss

Indexed keywords

CEFALEXIN; CONNEXIN 26; GENOMIC DNA; GENTAMICIN; RETINOID; RETINOL; SALICYLIC ACID;

ARTICLE; BLEPHARITIS; CASE REPORT; CHILD; COCHLEA PROSTHESIS; CONGENITAL MALFORMATION; CORNEA EPITHELIUM; CORNEA VASCULARIZATION; DANDY WALKER SYNDROME; EPIDERMIS; FEMALE; GENE MUTATION; HEARING IMPAIRMENT; HETEROZYGOTE DETECTION; HUMAN; HYPERKERATOSIS; ICTHIOSIS; KERATITIS; KERATOSIS, ICTHIOSIS AND DEAFNESS SYNDROME; MISSENSE MUTATION; NERVE POTENTIAL; NUCLEAR MAGNETIC RESONANCE IMAGING; PERCEPTION DEAFNESS; POSTOPERATIVE INFECTION; PRIORITY JOURNAL; SKIN DISEASE; WOUND COMPLICATION;

COCHLEAR IMPLANTATION; DANDY-WALKER SYNDROME; HEARING LOSS, BILATERAL; HEARING LOSS, SENSORINEURAL; HUMANS; ICHTHYOSIS; INFANT; KERATOSIS; SYNDROME;

EID: 41149163569     PISSN: 01655876     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ijporl.2008.01.017     Document Type: Article

References (22)

1. Propst E.J., Stockley T.L., Gordon K.A., Harrison R.V., and Papsin B.C. Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program. Int. J. Pediatr. Otorhinolaryngol. 70 3 (2006) 435-444
2. Burns F. A case of generalized congenital erythroderma. J. Cutan. Dis. 33 (1915) 255-260
3. Skinner B.A., Greist M.C., and Norins A.L. The keratitis, ichthyosis, and deafness (KID) syndrome. Arch. Dermatol. 117 5 (1981) 285-289
4. Caceres-Rios H., Tamayo-Sanchez L., Duran-Mckinster C., de la Luz Orozco M., and Ruiz-Maldonado R. Keratitis, ichthyosis, and deafness (KID syndrome): review of the literature and proposal of a new terminology. Pediatr. Dermatol. 13 2 (1996) 105-113
5. Lamprecht A., Goecke T., Anton-Lamprecht I., and Kuster W. Progressive erythrokeratodermia and cochlear hearing impairment: A case report and review of the literature. Int. J. Pediatr. Otorhinolaryngol. 15 3 (1988) 279-289
6. Hampton S.M., Toner J.G., and Small J. Cochlear implant extrusion in a child with keratitis, ichthyosis and deafness syndrome. J. Laryngol. Otol. 111 5 (1997) 465-467
7. Harms M., Gilardi S., Levy P.M., and Saurat J.H. KID syndrome (keratitis, ichthyosis, and deafness) and chronic mucocutaneous candidiasis: case report and review of the literature. Pediatr. Dermatol. 2 1 (1984) 1-7
8. Propst E.J., Blaser S., Stockley T.L., Harrison R.V., Gordon K.A., and Papsin B.C. Temporal bone imaging in GJB2 deafness. Laryngoscope 116 12 (2006) 2178-2186
9. Yotsumoto S., Hashiguchi T., Chen X., Ohtake N., Tomitaka A., Akamatsu H., et al. Novel mutations in GJB2 encoding connexin-26 in Japanese patients with keratitis-ichthyosis-deafness syndrome. Br. J. Dermatol. 148 4 (2003) 649-653
10. James A.L., and Papsin B.C. Device fixation and small incision access for pediatric cochlear implants. Int. J. Pediatr. Otorhinolaryngol. 68 8 (2004) 1017-1022
11. Szymko-Bennett Y.M., Russell L.J., Bale S.J., and Griffith A.J. Auditory manifestations of Keratitis-Ichthyosis-Deafness (KID) syndrome. Laryngoscope 112 2 (2002) 272-280
12. Tsuzuku T., Kaga K., Kanematsu S., Shibata A., and Ohde S. Temporal bone findings in keratitis, ichthyosis, and deafness syndrome. Case report. Ann. Otol. Rhinol. Laryngol. 101 5 (1992) 413-416
13. Myers E.N., Stool S.E., and Koblenzer P.J. Congenital deafness, spiny hyperkeratosis, and universal alopecia. Arch Otolaryngol. 93 1 (1971) 68-74
14. Boudghene-Stambouli O., Merad-Boudia A., and Abdelali S. KID syndrome, pachydermatoglyphy and Dandy-Walker syndrome. Ann. Dermatol. Venereol. 121 2 (1994) 99-102
15. Hsu H.C., Lin G.S., and Li W.M. Keratitis, ichthyosis, and deafness (KID) syndrome with cerebellar hypoplasia. Int. J. Dermatol. 27 10 (1988) 695-697
16. Zhang X.B., and Li C.X. A case of keratitis ichthyosis deafness (KID) syndrome associated with Dandy-Walker. J. Eur. Acad. Dermatol. Venereol. 21 5 (2007) 706-707
17. Chia L.G., and Li W.M. Clinical and electrophysiological studies in a patient with keratitis, ichthyosis and deafness (KID) syndrome. J. Neurogenet. 4 1 (1987) 57-64
18. Jurecka W., Aberer E., Mainitz M., and Jurgensen O. Keratitis, ichthyosis, and deafness syndrome with glycogen storage. Arch. Dermatol. 121 6 (1985) 799-801
19. van Geel M., van Steensel M.A., Kuster W., Hennies H.C., Happle R., Steijlen P.M., et al. HID and KID syndromes are associated with the same connexin 26 mutation. Br. J. Dermatol. 146 6 (2002) 938-942
20. Grob J.J., Breton A., Bonafe J.L., Sauvan-Ferdani M., and Bonerandi J.J. Keratitis, ichthyosis, and deafness (KID) syndrome. Vertical transmission and death from multiple squamous cell carcinomas. Arch. Dermatol. 123 6 (1987) 777-782
21. Kone-Paut I., Hesse S., Palix C., Rey R., Remediani K., Garnier J.M., et al. Keratitis, ichthyosis, and deafness (KID) syndrome in half sibs. Pediatr. Dermatol. 15 3 (1998) 219-221
22. Nazzaro V., Blanchet-Bardon C., Lorette G., and Civatte J. Familial occurrence of KID (keratitis, ichthyosis, deafness) syndrome: case reports of a mother and daughter. J. Am. Acad. Dermatol. 23 2 Pt 2 (1990) 385-388