Vohwinkel syndrome

Vohwinkel syndrome
Classification and external resources
OMIM	124500
DiseasesDB	32216
eMedicine	article/1108458

Vohwinkel syndome (also known as "Keratoderma hereditaria mutilans,"^[1] "Keratoma hereditaria mutilans,"^[1] "Mutilating keratoderma of Vohwinkel"^[2]:213, "Mutilating palmoplantar keratoderma"^[1]) is a diffuse autosomal dominant keratoderma with onset in early infancy characterized by a honeycombed keratoderma involving the palmoplantar surfaces.^[3]:512 Mild to moderate sensorineural hearing loss is often associated.^[3]:512

It has been associated with GJB2.^[4]

It was characterized in 1929.^[5]

See also

• Palmoplantar keratoderma
• List of cutaneous conditions

References

1. ^ ^{a b c} Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. pp. 779. ISBN 1-4160-2999-0. 
2. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0721629210.
3. ^ ^{a b} Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.
4. ^ Maestrini E, Korge BP, Ocaña-Sierra J, et al. (July 1999). "A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families". Hum. Mol. Genet. 8 (7): 1237–43. doi:10.1093/hmg/8.7.1237. PMID 10369869. http://hmg.oxfordjournals.org/cgi/pmidlookup?view=long&pmid=10369869. 
5. ^ Vohwinkel, K. H. Keratoma hereditarium mutilans. Arch. Derm. Syph. 158: 354-364, 1929.

This cutaneous condition article is a stub. You can help Wikipedia by expanding it.v · Categories: Cutaneous condition stubs Palmoplantar keratodermas Wikimedia Foundation. 2010. Игры ⚽ Нужен реферат? Olmsted syndrome Mutilation (demo) Look at other dictionaries: Vohwinkel syndrome — Voh·win·kel syndrome (fo vingґkəl) [Karl Hermann Vohwinkel, German dermatologist, 20th century] see under syndrome …   Medical dictionary Vohwinkel syndrome — an autosomal dominant, progressive form of palmoplantar keratoderma that begins in childhood, characterized by a stellate pattern of hyperkeratosis on the backs of the hands and feet, linear keratoses on elbows and knees, and annular… …   Medical dictionary syndrome — The aggregate of symptoms and signs associated with any morbid process, and constituting together the picture of the disease. SEE ALSO: disease. [G. s., a running together, tumultuous concourse; (in med.) a concurrence of symptoms, fr. syn,… …   Medical dictionary Vohwinkel — H.H., 20th century German dermatologist. See V. syndrome …   Medical dictionary Kindler syndrome — Classification and external resources OMIM 173650 DiseasesDB 32778 eMedicine …   Wikipedia Ellis–van Creveld syndrome — Classification and external resources Polydactyly in Ellis–van Creveld syndrome ICD 10 Q …   Wikipedia Naegeli–Franceschetti–Jadassohn syndrome — Classification and external resources OMIM 161000 DiseasesDB 29767 eMedicine …   Wikipedia Hallermann–Streiff syndrome — Classification and external resources ICD 9 756.0 OMIM 234100 DiseasesDB …   Wikipedia Jervell and Lange-Nielsen syndrome — Classification and external resources ICD 9 426.82 OMIM 220400 DiseasesDB …   Wikipedia Netherton syndrome — Classification and external resources ICD 10 Q80.8 (ILDS Q80.870) ICD 9 757.1 OMIM …   Wikipedia 18+ © Academic, 2000-2024 Contact us: Technical Support, Advertising Dictionaries export, created on PHP, Joomla, Drupal, WordPress, MODx. Mark and share Search through all dictionaries Translate… Search Internet Share the article and excerpts Direct link … Do a right-click on the link above and select “Copy Link”