Cargando…

Progressive Symmetric Erythrokeratoderma Having Overlapping Features With Erythrokeratoderma Variabilis and Lesional Hypertrichosis: Is Nomenclature “Erythrokeratoderma Variabilis Progressiva” More Appropriate?

Detalles Bibliográficos
Autores principales:	Mahajan, Vikram K, Khatri, Gayatri, Chauhan, Pushpinder S, Mehta, Karaninder S, Raina, Rashmi, Gupta, Mrinal
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Medknow Publications & Media Pvt Ltd 2015
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533547/ https://www.ncbi.nlm.nih.gov/pubmed/26288417 http://dx.doi.org/10.4103/0019-5154.160499

Ejemplares similares

Dermoscopy of Erythrokeratoderma Variabilis
por: Neema, Shekhar, et al.
Publicado: (2020)

Erythrokeratoderma variabilis (EKV) – First Nepalese case documenting GJB3 mutation
por: Shah, M., et al.
Publicado: (2021)

Progressive Symmetric Erythrokeratoderma with Unusual Associations
por: Chander, Ram, et al.
Publicado: (2014)

Progressive Symmetrical Erythrokeratoderma Associated with Punctate Palmoplantarkeratoderma
por: Tiwary, Anup K., et al.
Publicado: (2019)

Late Onset Progressive Symmetric Erythrokeratoderma with Pseudo Ainhum
por: Asha, Gowrappala Shanmukhappa, et al.
Publicado: (2016)

Progressive symmetric erythrokeratoderma with nephrotic syndrome: Coincidence or new association?
por: Sacchidanand, S, et al.
Publicado: (2013)

Progressive and symmetric erythrokeratoderma of adult onset: A rare case
por: Prabhu, Smitha, et al.
Publicado: (2010)

Progressive symmetrical erythrokeratoderma on the face: A rare condition and successful treatment with calcipotriol
por: Tarikci, Nagihan, et al.
Publicado: (2016)

Analysis of TYR Gene Pathogenic Variants in a Chinese Mongolian Family with Progressive Symmetric Erythrokeratoderma
por: Duan, Yan, et al.
Publicado: (2021)

Erythrokeratodermia variabilis with hypertrichosis on the lesions
por: Wu, Jian-Ping, et al.
Publicado: (2020)

Progressive symmetrical erythrokeratoderma manifesting as harlequin-like ichthyosis with severe thrombocytopenia secondary to a homozygous 3-ketodihydrosphingosine reductase mutation
por: Altawil, Lama, et al.
Publicado: (2021)

Transgenic Mice Expressing a Mutant Form of Loricrin Reveal the Molecular Basis of the Skin Diseases, Vohwinkel Syndrome and Progressive Symmetric Erythrokeratoderma
por: Suga, Yasushi, et al.
Publicado: (2000)

Integration of Phenotype Term Prioritization and Gene Expression Analysis Reveals a Novel Variant in the PERP Gene Associated with Autosomal Recessive Erythrokeratoderma
por: González-Quintana, Adrián, et al.
Publicado: (2023)

Interrogation of Carboxy-Terminus Localized GJA1 Variants Associated with Erythrokeratodermia Variabilis et Progressiva
por: Lucaciu, Sergiu A., et al.
Publicado: (2022)

Two de novo GJA1 mutation in two sporadic patients with erythrokeratodermia variabilis et progressiva
por: Li, Changxing, et al.
Publicado: (2019)

Apophysomyces variabilis Infections in Humans
por: Guarro, Josep, et al.
Publicado: (2011)

Dominant de novo mutations in GJA1 cause erythrokeratodermia variabilis et progressiva, without features of oculodentodigital dysplasia
por: Boyden, Lynn M., et al.
Publicado: (2014)

Exome sequencing identifies novel compound heterozygous mutations in GJB3 gene that cause erythrokeratodermia variabilis et progressiva
por: Deng, Yongqiong, et al.
Publicado: (2018)

L’osservazione delle stelle variabili
por: Good, Gerry A
Publicado: (2008)

Erythrokeratodermia variabilis: Two case reports
por: Karadag, Ayse Serap, et al.
Publicado: (2013)

A Case of Erythrokeratodermia Variabilis in Korean
por: Oh, Dae Young, et al.
Publicado: (2019)

Ritmi circadiani e variabili metaboliche
por: Benazzi, Sara, et al.
Publicado: (2021)

A Rare Case of Apophysomyces Variabilis Skin and Soft Tissue Infection
por: Bora, Archana, et al.
Publicado: (2021)

Two Furanosesterterpenoids from the Sponge Luffariella variabilis
por: Ahmadi, Peni, et al.
Publicado: (2017)

Biological characteristics and fungicide sensitivity of Pyricularia variabilis
por: Zhang, Yiming, et al.
Publicado: (2021)

Spotted-Fever Group Rickettsia in Dermacentor variabilis, Maryland
por: Ammerman, Nicole C., et al.
Publicado: (2004)

Teoria della probabilità: variabili aleatorie e distribuzioni
por: Pascucci, Andrea
Publicado: (2020)

Complete genome sequence of Anabaena variabilis ATCC 29413
por: Thiel, Teresa, et al.
Publicado: (2014)

Necrotizing fasciitis caused by Apophysomyces variabilis in an immunocompetent patient
por: Rodríguez, José Y., et al.
Publicado: (2017)

Free Radical Scavenging Activity of Kielmeyera variabilis (Clusiaceae)
por: Coqueiro, Aline, et al.
Publicado: (2013)

Complete mitochondrial genome of Quercus variabilis (Fagales, Fagaceae)
por: Bi, Quanxin, et al.
Publicado: (2019)

Bier spots: An uncommon cause of mottled skin
por: Mahajan, Vikram K, et al.
Publicado: (2015)

Aggressive cutaneous zygomycosis caused by Apophysomyces variabilis in an immunocompetent child
por: Al-Zaydani, Ibrahim A., et al.
Publicado: (2015)

Comparative vertical transmission of Rickettsia by Dermacentor variabilis and Amblyomma maculatum
por: Harris, Emma K., et al.
Publicado: (2017)

Ceratocystis quercicola sp. nov. from Quercus variabilis in Korea
por: Cho, Sung-Eun, et al.
Publicado: (2020)

Necrotizing fasciitis caused by Apophysomyces variabilis in a burn patient
por: Samaddar, Arghadip, et al.
Publicado: (2019)

The genome sequence of the Figwort Cheilosia, Cheilosia variabilis (Panzer, 1798)
por: Crowley, Liam M., et al.
Publicado: (2023)

Partial Loss of Function ABCA12 Mutations Generate Reduced Deposition of Glucosyl-Ceramide, Leading to Patchy Ichthyosis and Erythrodermia Resembling Erythrokeratodermia Variabilis et Progressiva (EKVP)
por: Terrinoni, Alessandro, et al.
Publicado: (2023)

Zinc Therapy in Dermatology: A Review
por: Gupta, Mrinal, et al.
Publicado: (2014)

Hair dye dermatitis and p-phenylenediamine contact sensitivity: A preliminary report
por: Gupta, Mrinal, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_vm89hk377h176icv030vrg2cck