Disease: Pachyonychia congenita Jackson Lawler type
- [[Translated article]]Congenital and Hereditary Nail Disease
- A case of pachyonychia congenita with a hotspot variant at Arg127 in KRT16: Disease severity assessment using AlphaMissense technology
- A cross-sectional study of erythromelalgia in patients with pachyonychia congenita
- A KRT16 mutation in the first Chinese pedigree with Pachyonychia congenita and review of the literatures
- A KRT6A and a Novel KRT16 Gene Mutations in Chinese Patients with Pachyonychia Congenita
- A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case report
- A novel heterozygous frameshift mutation in the KRT6A gene responsible for an uncommon phenotype of pachyonychia congenita: One case report and review of literature
- A novel KRT16 frameshift variant causing pachyonychia congenita by re-initiation of translation
- A Rare Case of Pachyonychia Congenita and the Need for Awareness
- A recurrent missense mutation in the KRT16 gene causing pachyonychia congenita in a patient
- A role for keratins in supporting mitochondrial organization and function in skin keratinocytes
- A simple modified surgical technique combined with tissue adhesive for steatocystoma multiplex
- A systematic review of reported cases of pachyonychia congenita tarda
- A treatment protocol for botulinum toxin injections in the treatment of pachyonychia congenita-associated keratoderma
- A unique skin phenotype resulting from a large heterozygous deletion spanning six keratin genes
- Altered keratinocyte differentiation is an early driver of keratin mutation-based palmoplantar keratoderma
- Coexistence of Hidradenitis Suppurativa and Steatocystoma Multiplex: Is It a New Variant of Hidradenitis Suppurativa?
- Coexistence of pachyonychia congenita and hidradenitis suppurativa: more than a coincidence
- Coexistence of steatocystoma multiplex and hidradenitis suppurativa: Assessment of this unique association by means of ultrasonography and Color Doppler
- Congenital and Hereditary Nail Disease
- Congenital nail abnormalities
- Correction: Genetic variants in pachyonychia congenita-associated keratins increase susceptibility to tooth decay
- Current mysteries of pachyonychia congenita
- Defining patient-centered research priorities in pediatric dermatology
- Dermpath & Clinic: Multiple nodules in the axillae: is it that old chestnut Hidradenitis suppurativa again?
- Distinctions in the Management, Patient Impact, and Clinical Profiles of Pachyonychia Congenita Subtypes
- EGFR Signaling Is Overactive in Pachyonychia Congenita: Effective Treatment with Oral Erlotinib
- Familial neurofibromatosis type 1 has diverse manifestations in skin and is associated with steatocystoma multiplex
- Follicular occlusion tetrad in a male patient with pachyonychia congenita: clinical and genetic analysis
- Future Perspectives of Oral Delivery of Next Generation Therapies for Treatment of Skin Diseases
- Generalized bullae in a young girl with KRT6A-related pachyonychia congenita
- Genetic and developmental disorders of the oral mucosa: Epidemiology; molecular mechanisms; diagnostic criteria; management
- Genetic study of a Chinese pedigree affected with pachyonychia congenita
- Genotype-phenotype correlations of neurovascular structures on the feet in patients with pachyonychia congenita: A cross-sectional study
- Genotype-Structurotype-Phenotype Correlations in Patients with Pachyonychia Congenita
- Genotype‒Structurotype‒Phenotype Correlations in Patients with Pachyonychia Congenita
- Heterozygous variants in the integrin subunit beta 4 gene (ITGB4) cause autosomal dominant nail dystrophy
- Highly branched poly(β-amino ester)s for gene delivery in hereditary skin diseases
- Homozygous dominant missense mutation in Keratin 6b leading to severe pachyonychia congenita
- Identification of clinically useful predictive genetic variants in pachyonychia congenita
- Imaging features of steatocystoma multiplex- back to basics
- Increase in melanoma knowledge in Latino patients after a targeted digital educational program
- Intravenous Ketamine as an Adjunct for Pachyonychia Congenita-Associated Pain: A Case Report
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Keratin 6a mutations lead to impaired mitochondrial quality control
- Management of symptomatic mucosal involvement in paediatric pachyonychia congenita
- Modulation of keratin deposition and pathogenesis of hidradenitis suppurativa: evidence coming from pachyonychia congenita
- Molecular epidemiology of pachyonychia congenita in the Israeli population
- Multiple human papillomavirus-associated plantar epidermoid cysts
- Mutation analysis of the KRT17 gene in steatocystoma multiplex and a brief literature review
- Mutation p.Arg127Pro in the 1A Domain of KRT16 Causes Pachyonychia Congenita in Chinese Patient: A Case Report of PC Associated with Acral Melanoma
- Nail Whispers Revealing Dermatological and Systemic Secrets: An Analysis of Nail Disorders Associated With Diverse Dermatological and Systemic Conditions
- Novel mutations in desmoglein 1: focal palmoplantar keratoderma in milder phenotypes
- Numerous flesh-colored nodules on the trunk
- Ocular manifestations of skin diseases with pathological keratinization abnormalities
- Old mitochondria accumulate in pachyonychia congenita
- Pachyonychia Congenita
- Pachyonychia congenita - pathogenesis of pain and approaches to treatment
- Pachyonychia congenita and botulinum toxin
- Pachyonychia Congenita Associated with a Novel Variant of KRT17 Presenting Unusual Oral Manifestations
- Pachyonychia Congenita Project: Advancing Research and Drug Development through Collaboration
- Pachyonychia congenita responding favorably to a combination of surgical and medical therapies
- Pachyonychia Congenita with a Novel Variant in the <em>KRT16</em> Gene, c.348_379delinsAA
- Pachyonychia Congenita with a Novel Variant in the KRT16 Gene, c.348_379delinsAA
- Pachyonychia congenita, a paradigm for rare skin disorders
- Pachyonychia congenita: A father and son with a novel variant in the KRT16 gene
- Pachyonychia Congenita: A Research Agenda Leading to New Therapeutic Approaches
- Pachyonychia Congenita: Clinical Features and Future Treatments
- Pachyonychia congenita: Spectrum of cutaneous disease
- Pachyonychia Congenita: Sporadic Onset with Mutation Analysis
- Pain Hypersensitivity in SLURP1 and SLURP2 Knock-out Mouse Models of Hereditary Palmoplantar Keratoderma
- PAIN HYPERSENSITIVITY IN SLURP1 AND SLURP2 KNOCKOUT MOUSE MODELS OF HEREDITARY PALMOPLANTAR KERATODERMA
- Painful thickened skin on the soles of the feet
- Pathophysiology of pachyonychia congenita-associated palmoplantar keratoderma: new insights into skin epithelial homeostasis and avenues for treatment
- Pediatric Nail Disorders
- Phenotype and genotype features of Vietnamese children with pachyonychia congenita
- Plantar pain and thickened nails: a genodermatosis
- Posttranslational modifications of keratins and their associated proteins as therapeutic targets in keratin diseases
- Prevalence and Characterization of Itch in Pachyonychia Congenita
- Proteomic profiling reveals KRT6C as a probable hereterodimer partner for KRT9: New insights into re-classifying epidermolytic palmoplantar keratoderma (EPPK) and a milder form of pachyonychia congenita (PC-K6c) as a group of genetic cutaneous disorders
- Revisiting pachyonychia congenita: a case-cohort study of 815 patients
- Scrotal Tumoral Calcinosis: A Rare and Easily Misdiagnosed Situation
- Scrutinising the role of simvastatin in a patient of Pachyonychia Congenita with KRT6A gene mutation
- Severely Callused Hands and Feet
- Sharing (data) is caring for patients with pachyonychia congenita
- Steatocystoma multiplex suppurativa associated with hidradenitis suppurativa successfully treated with adalimumab
- Stopping pachyonychia congenita plantar pain with a statin?
- Successful treatment of Pachyonychia congenita with Rosuvastatin
- Successful treatment of pachyonychia congenita with simvastatin
- Surgical Management of Pachyonychia Congenita in a 3-Year-Old
- Symptomatic mucosal involvement in pachyonychia congenita: challenges in infants and young children
- The histopathological features of the nail plate in pachyonychia congenita
- The Pachyonychia Congenita Virtual Support Group Meeting: Patient Insights and Pearls
- The rationale of ideal pulse duration and pulse interval in the treatment of steatocystoma multiplex using the carbon dioxide laser in a super-pulse mode as opposed to the ultra-pulse mode
- Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review
- Treatment of Painful Palmoplantar Keratoderma Related to Pachyonychia Congenita Using EGFR Inhibitors
- Ultrasound Morphologic Features of Steatocystoma Multiplex With Clinical Correlation
- Ultrasound-Guided Intralesional Cryotherapy for Treatment of Steatocystoma Multiplex
- Update on pachyonychia congenita research
- Walking a day in a pachyonychia congenita patient's shoes: Impact on plantar pain and activity levels measured with wristband activity trackers