Genodermatosis: Update on Pathogenesis and Clinical Sequencing: The Journal of Dermatology: Vol 52, No 3

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The Journal of Dermatology: Volume 52, Issue 3

Genodermatosis: Update on Pathogenesis and Clinical Sequencing

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ISSUE INFORMATION

Issue Information

GUEST EDITORIAL

Perspectives and history in genodermatoses

REVIEW

Genodermatosis: Update on Pathogenesis and Clinical Sequencing

Advanced phasing techniques in congenital skin diseases

Updated genetic background of generalized pustular psoriasis as an autoinflammatory keratinization disease

History and prospects of Nagashima-type palmoplantar keratosis, the most common palmoplantar keratoderma in east Asian populations

ORIGINAL ARTICLE

Real-world assessment of the patient profile, clinical characteristics, treatment patterns, and outcomes associated with erythropoietic and X-linked protoporphyria

Repurposing diacerein for the treatment of chronic wounds in recessive-dystrophic epidermolysis bullosa patients by modulating matrix metalloproteinase-9 expression

The impact of antibiotic therapy in psoriasis patients with active streptococcal infection: A prospective study

Validation of Laboratory Risk Indicator for Necrotizing Fasciitis (LRINEC) score and establishment of novel score in Japanese patients with necrotizing fasciitis (J-LRINEC score)

Dermatopathological features and successful treatment with topical antioxidant for ichthyosiform lesions in Mitchell syndrome caused by an ACOX1 variant

Traumatic experiences, dissociative symptoms, and alexithymia in patients with alopecia areata

Comorbid diseases in bullous pemphigoid: A population-based case–control study

Experimental method for creating skin with acquired appendage dysfunction

Inflammatory proteins and hidradenitis suppurativa: Insights from genetic correlation and Mendelian randomization

The genomic landscape of cutaneous squamous cell carcinoma in Japan

Epidemiological insights into chronic urticaria, vitiligo, alopecia areata, and herpes zoster following COVID-19 infection: A nationwide population-based study

CONCISE COMMUNICATION

Coincidence of acral peeling skin syndrome and Nagashima-type palmoplantar keratosis in a Japanese pedigree with acral skin peeling

Using patient preference to inform ritlecitinib dose selection for alopecia areata treatment

Novel pathogenic variants in HR underlie atrichia with papular lesions in a cohort of 10 families

Clinical and genetic insights into ABCA12 variants in three Chinese families with ichthyosis: Genotype–phenotype correlation

A case of peeling skin syndrome type 1 with novel CDSN gene variation successfully treated with upadacitinib

Biallelic pathogenic variants in the LSS gene cause congenital alopecia-cataract syndrome

Onychomycosis caused by Aspergillus species belonging to section Circumdati

Kodamaea ohmeri infection can be the causative agent of secondary infections of intertrigo: A case study

Phenotypic and genotypic analysis of SERPINA12-related autosomal recessive palmoplantar keratoderma in southwestern China

Predictive factors for responders to deucravacitinib treatment in patients with psoriasis

RESEARCH NOTE

Infiltration of M2a macrophages is predominant in genital verruciform xanthoma

Identification of key malodor components in onychomycosis: A pilot study

Significance of cell adhesion molecule 1 expression in mycosis fungoides: Diagnostic implications and clinical correlations

Intravenous immunoglobulin inhibits neutrophil extracellular traps in Stevens-Johnson syndrome/toxic epidermal necrolysis

ISSUE INFORMATION

Issue Information

GUIDELINES

Guidelines for the management of drug-induced hypersensitivity syndrome 2023

IMAGES IN DERMATOLOGY

Lymphomatoid papulosis type E: An indolent diagnosis in disguise

LETTER TO THE EDITOR

Novel compound heterozygous MPDU1 variants causing congenital disorders of glycosylation presenting with erythrokeratodermia variabilis

Nagashima-type palmoplantar keratosis patients harboring SERPINB7 and SERPINA12 variants

A mutation in the SREBF1 gene resulting in autosomal-dominant ichthyosis Follicularis, Atrichia, and photophobia syndrome

Remission of intercellular IgG/IgA dermatosis after treatment for cervical cancer

A case of Darier's disease with a missense mutation in exon 8 of ATP2A2

Pasteurella stomatis and Prevotella heparinolytica infection following dog bite. A case report and review of published works

A case of solar urticaria complicated by eosinophilic granulomatosis with polyangiitis treated with mepolizumab

Association between nail psoriasis and obesity: A cross-sectional study at a single institution

Anti-transcription intermediate factor 1-γ antibody-positive dermatomyositis with refractory skin ulcers and rapid cancer progression

Two cases of lichen planus pigmentosus inversus improved by topical tacrolimus application and the avoidance of tight clothing

Segmental lichen aureus: A case report of zosteriform distribution and severe pain with literature review

Comparing the severity of epidermolysis bullosa simplex harboring KRT5 variants with the AlphaMissense score

Effective management of coexisting bullous pemphigoid and psoriasis with bimekizumab

The first Japanese case of intractable tinea corporis caused by Trichophyton indotineae

BRAF/MEK inhibitor-induced tumor lysis syndrome in a patient with malignant melanoma

A case of crateriform verruca on the right sole without human papilloma virus detection

A case of mucous membrane pemphigoid solely with IgA anti-BP230 antibodies detected by immunoblotting using normal human epidermal extracts

A case of digital papillary adenocarcinoma with human papillomavirus 42 detected

Hematologic diseases in patients with cutaneous sarcoidosis

Plate-like osteoma cutis along Blaschko line: A case report and published work review of lesion distribution

Is alopecia areata one of the atopic diseases? A two-sample Mendelian randomization analysis

A case of bullous pemphigoid after nemolizumab administration

Potential sitosterolemia in necrobiotic xanthogranuloma: Comment on “Extensive yellowish masses in bilateral orbit and neck”

Response to: “Potential sitosterolemia in necrobiotic xanthogranuloma: Comment on Extensive yellowish masses in bilateral orbit and neck” by Chen et al.

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