Keratosis punctata palmaris et plantaris

Keratosis punctata palmaris et plantaris
Keratosis punctata palmaris et plantaris
Classification and external resources
ICD-10 L85.2
OMIM 148600
DiseasesDB 32839

Keratosis punctata palmaris et plantaris (also known as "Autosomal-dominant hereditary punctate keratoderma associated with malignancy," "Buschke–Fischer–Brauer disease," "Davis Colley disease," "Keratoderma disseminatum palmaris et plantaris," "Keratosis papulosa," "Keratoderma punctatum," "Keratodermia punctata," "Keratoma hereditarium dissipatum palmare et plantare," "Palmar and plantar seed dermatoses," "Palmar keratoses," "Papulotranslucent acrokeratoderma," "Punctate keratoderma," "Punctate keratoses of the palms and soles," and "Maculosa disseminata") is a skin condition, an autosomal dominant palmoplantar keratoderma with variable penetrance, characterized clinically by multiple, tiny, punctate keratoses over the entire palmoplantar surfaces, beginning over the lateral edge of the digits.[1]:509[2]:212-213

It has been linked to 15q22-q24.[3]

See also

References

  1. ^ Freedberg, et al. (2003). Fitzpatrick's Dermatology in General Medicine. (6th ed.). McGraw-Hill. ISBN 0071380760.
  2. ^ James, William; Berger, Timothy; Elston, Dirk (2005). Andrews' Diseases of the Skin: Clinical Dermatology. (10th ed.). Saunders. ISBN 0721629210.
  3. ^ Martinez-Mir A, Zlotogorski A, Londono D, et al. (December 2003). "Identification of a locus for type I punctate palmoplantar keratoderma on chromosome 15q22-q24". J. Med. Genet. 40 (12): 872–8. doi:10.1136/jmg.40.12.872. PMC 1735333. PMID 14684683. http://jmg.bmj.com/cgi/pmidlookup?view=long&pmid=14684683. 
Dermis/
localized CTD

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