A “new” autosomal dominant genodermatosis characterized by hyperpigmented spots and palmo- plantar hyperkeratosis

Author:

Cantú J. M.,Sánchez-Corona J.,Fragoso R.,Macotela-Ruiz E.,García-Cruz D.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference8 articles.

1. Intestinal polyposis associated with mucocutaneous pigmentation;Bartholomew;Surg. Gynec. Obstet.,1962

2. Multiple lentiginosis syndrome. Complex comprising multiple lentiginosis, electrocardiographic conduction abnormalities of genitalia, retardation of growth, sensorineural deafness, and autosomal dominant hereditary pattern;Gorlin;Amer. J. Dis. Child.,1969

3. Neurocutane Melanosen. Z;Herzberg;Kinderchir.,1965

4. Acrokeratoelastoidosis;Jung;Hum. Genet.,1973

5. A pedigree of generalized lentigo;Pipkin;J. Hered.,1950

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1. Hyperpigmentations;Annales de Dermatologie et de Vénéréologie;2019-10

2. Hereditary palmoplantar keratodermas. Part I. Non-syndromic palmoplantar keratodermas: classification, clinical and genetic features;Journal of the European Academy of Dermatology and Venereology;2018-03-24

3. Hiperpigmentaciones;EMC - Dermatología;2017-09

4. Guttate Hypopigmentation and Punctate Palmoplantar Keratoderma;Challenging Cases in Dermatology;2012-09-04

5. Disorders of Skin Colour;Rook's Textbook of Dermatology;2010-05-06

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