Wildervanck syndrome
(Redirected from Franceschetti–Klein–Wildervanck syndrome)
| Wildervanck syndrome | |
|---|---|
| Other names | Cervicooculoacoustic syndrome[1] |
| Specialty | Neurology |
Wildervanck syndrome or cervico-oculo-acoustic syndrome comprises a triad of:[2][3]
- Duane syndrome
- Klippel-Feil anomaly (fused cervical vertebrae)
- congenital hearing loss
Wildervanck syndrome is a developmental disorder that may be characterized by accessory tragi.[4][5]
References
[edit]- ^ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Wildervanck syndrome". www.orpha.net. Retrieved 28 April 2019.
{{cite web}}: CS1 maint: numeric names: authors list (link) - ^ "OMIM Entry-314600 - WILDERVANCK SYNDROME".
- ^ "Wildervanck Syndrome".
- ^ Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. p. 894. ISBN 978-1-4160-2999-1.
- ^ Mehta, B; Nayak, C; Savant, S; Amladi, S (2007). "Goldenhar syndrome with unusual features". Indian Journal of Dermatology, Venereology and Leprology. 74 (3): 254–6. doi:10.4103/0378-6323.41374. hdl:1807/48126. PMID 18583796.
External links
[edit]
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