Erythrokeratodermia with ataxia
(Redirected from Giroux–Barbeau syndrome)
| Erythrokeratodermia with ataxia | |
|---|---|
| Other names | Giroux–Barbeau syndrome[1] |
 | |
| Erythrokeratodermia with ataxia is inherited in an autosomal dominant fashion. | |
| Specialty | Medical genetics |
Erythrokeratodermia with ataxia is a condition characterized by erythematous, hyperkeratotic plaques with fine, white, attached scales distributed almost symmetrically on the extremities.[1]
See also
[edit]References
[edit]- ^ a b Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.