Palmoplantar keratoderma and spastic paraplegia

Palmoplantar keratoderma and spastic paraplegia
Palmoplantar keratoderma and spastic paraplegia
Classification and external resources
OMIM 148360

Palmoplantar keratoderma and spastic paraplegia (also known as "Charcot–Marie–Tooth disease with palmoplantar keratoderma and nail dystrophy"[1]) is an autosomal dominant or x-linked dominant condition that begins in early childhood with thick focal keratoderma over the soles and, to a lesser extent, the palms.[1]:513

See also

References

  1. ^ a b Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.