Mal de Meleda: A Focused Review

Comment on Zhao et al. “Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda”

(2015) R Nellen et al.   ACTA DERMATO-VENEREOLOGICA

Costello-Syndrom

(2015) M. Wirtz et al.   HAUTARZT

A novel mutation in SLURP1 in patients with mal de Meleda from the Indian subcontinent

(2015) Ruud G.L. Nellen et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

First Mal de Meleda report in Chinese Mainland: two families with a recurrent homozygous missense mutation in SLURP-1

(2015) J. Zhang et al.   JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY

Olmsted syndrome: clinical, molecular and therapeutic aspects

(2015) Sabine Duchatelet et al.   Orphanet Journal of Rare Diseases

Palmoplantar Keratoderma of the Gamborg-Nielsen Type is Caused by Mutations in the SLURP1 Gene and Represents a Variant of Mal de Meleda

(2014) L Zhao et al.   ACTA DERMATO-VENEREOLOGICA

Mal de Meleda in Indonesia: Mutations in theSLURP1gene appear to be ubiquitous

(2014) Jessica A Taylor et al.   AUSTRALASIAN JOURNAL OF DERMATOLOGY

A Japanese case of Mal de Meleda withSLURP1mutation

(2014) Jun-ichi Sakabe et al.   JOURNAL OF DERMATOLOGY

Palmoplantar Keratoderma along with Neuromuscular and Metabolic Phenotypes in Slurp1 -Deficient Mice

(2014) Oludotun Adeyo et al.   JOURNAL OF INVESTIGATIVE DERMATOLOGY

Mutations in SERPINB7, Encoding a Member of the Serine Protease Inhibitor Superfamily, Cause Nagashima-type Palmoplantar Keratosis

(2013) Akiharu Kubo et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Haplotype analysis in western European patients with mal de Meleda: founder effect for the W15R mutation in theSLURP1gene

(2013) R.G.L. Nellen et al.   BRITISH JOURNAL OF DERMATOLOGY

Particular Mal de Meleda Phenotypes in Tunisia and Mutations Founder Effect in the Mediterranean Region

(2013) Mbarka Bchetnia et al.   Biomed Research International

Mal de Meleda with lip involvement: A report of two cases

(2012) DevinderMohan Thappa et al.   INDIAN JOURNAL OF DERMATOLOGY

Mal de Meleda: relato de 2 casos de ocorrência familiar

(2011) Fernanda Ayres de Morais e Silva et al.   ANAIS BRASILEIROS DE DERMATOLOGIA

A Sporadic Case of Mal de Meleda Caused by Gene Mutation in SLURP-1 in Korea

(2011) Young Jae Oh et al.   Annals of Dermatology

A Novel Homozygous Missense Mutation in SLURP1 Causing Mal de Meleda With an Atypical Phenotype

(2011) Robert Gruber et al.   ARCHIVES OF DERMATOLOGY

SLURP1 mutation-impaired T-cell activation in a family with mal de Meleda

(2010) J-W. Tjiu et al.   BRITISH JOURNAL OF DERMATOLOGY

Palmoplantar keratoderma - Mal de Meleda syndrome

(2010) Nadiga Rajashekhar et al.   INTERNATIONAL JOURNAL OF DERMATOLOGY

Mutations in the SLURP-1 gene underlie Mal de Meleda in three Pakistani families

(2009) Muhammad Wajid et al.   JOURNAL OF DERMATOLOGICAL SCIENCE

Melanoma in skin affected with keratoderma palmoplantaris hereditaria (Mal de Meleda): Treatment with excision and grafting

(2009) Leonardo Sartore et al.   JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY

Peut-on traiter chirurgicalement le Mal de Meleda (kératodermie palmoplantaire diffuse de Siemens) ?

(2008) A. Marchac et al.   Annales de Chirurgie Plastique Esthetique

Compound heterozygosity for ARS component B mutations in a Dutch patient with mal de Meleda

(2008) R.G.L. Nellen et al.   BRITISH JOURNAL OF DERMATOLOGY