Erythrokeratodermia with ataxia

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

• Hallerman–Streiff syndrome
• List of cutaneous conditions

References

1. Rapini, Ronald P.; Bolognia, Jean L.; Jorizzo, Joseph L. (2007). Dermatology: 2-Volume Set. St. Louis: Mosby. ISBN 978-1-4160-2999-1.

External links