Erythrokeratodermia with ataxia

Erythrokeratodermia with ataxia
Other namesGiroux–Barbeau syndrome[1]
Erythrokeratodermia with ataxia is inherited in an autosomal dominant fashion.
SpecialtyMedical 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

References

  1. ^ 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.
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