• A case of Carvajal syndrome presenting with dilated cardiomyopathy
• A case of pachyonychia congenita with a hotspot variant at Arg127 in KRT16: Disease severity assessment using AlphaMissense technology
• A Case of Palmoplantar Keratoderma in the Constellation of Connective Tissue Diseases
• A mutation in CCDC91, Homo sapiens coiled-coil domain containing 91 protein, cause autosomal-dominant acrokeratoelastoidosis
• A novel FAM83G variant from palmoplantar keratoderma patient disrupts WNT signalling via loss of FAM83G-CK1alpha interaction
• A novel heterozygous frameshift mutation in the <em>KRT6A</em> gene responsible for an uncommon phenotype of pachyonychia congenita: One case report and review of literature
• A novel mutation in SLURP1 in patients with Mal de Meleda from Turkey
• A novel SERPINA12 variant and first European patients with diffuse palmoplantar keratoderma
• A Novel Variant in the <em>Desmoplakin</em> Gene in One Case of the Rare Carvajal Syndrome with Dilated Cardiomyopathy: A Case Report and Literature Review
• A Rare Case on Capecitabine Induced Acquired Palmoplantar Keratoderma
• A role for aquaporin-5 mutations in regulation of the actin cytoskeleton in non-epidermolytic palmoplantar keratoderma
• A Role for Aquaporin-5 Variants in Regulation of the Actin Cytoskeleton in Non-Epidermolytic Palmoplantar Keratoderma
• Acquired diffuse palmoplantar erythema with keratoderma in Chinese patients with pustular psoriasis: A predictor for IL36 receptor antagonist c.115+6T>C mutation?
• Acrokeratoelastoidosis
• Aesthetic oral rehabilitation of the upper-anterior sector with supra-nano filling resin in a patient with woolly hair syndrome: case report
• An Institution Based Cross-Sectional Observational Aetiological Study Correlating the Clinico-Pathological Findings in Patients Presenting with Acquired Palmoplantar Keratoderma
• Aquagenic keratoderma: A rare disease in the COVID age?
• Aquagenic keratoderma: three case reports
• Atypical Mal de Meleda in a Hispanic Patient
• Autosomal recessive plantar keratoderma with ragged periungual hyperkeratosis caused by a homozygous missense variant in KRT16
• Bilateral Burning Palmoplantar Lesions
• Calcium Regulation of Connexin Hemichannels
• Case report of crusted scabies, brief review of its pathophysiology and latest data
• Case report: Area of focus of management of severe pityriasis rubra pilaris by dose optimization of adalimumab biosimilar in combination with acitretin and montelukast
• CASTing the net wider: A case report of PLACK syndrome associated with dilated cardiomyopathy
• Cathepsin C in health and disease: from structural insights to therapeutic prospects
• Cathepsin C role in inflammatory gastroenterological, renal, rheumatic, and pulmonary disorders
• Cleavage of the pseudoprotease iRhom2 by the signal peptidase complex reveals an ER-to-nucleus signaling pathway
• Clinical and Histopathological Findings in Palmoplantar Lichen Planus Presenting as Diffuse Keratoderma
• Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation
• Cohen syndrome coincident with epidermolytic palmoplantar keratoderma caused by novel KRT9 gene mutation: A rare case report
• Cohen syndrome combined with novel KRT9 gene mutation leading to epidermolytic palmoplantar keratoderma: A rare case report
• Cornu Cutaneum: Case Reports of Patients With a Cutaneous Horn Associated With Either a Verruca Vulgaris or an Inverted Follicular Keratosis and a Review of the Etiologies of Cutaneous Horns
• Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients
• Disruption of TUFT1, a Desmosome-Associated Protein, Causes Skin Fragility, Woolly Hair, and Palmoplantar Keratoderma
• Disruption of tuftelin 1, a desmosome associated protein, causes skin fragility, woolly hair and palmoplantar keratoderma
• ECFS standards of care on CFTR-related disorders: Identification and care of the disorders
• Epidermal growth factor receptor inhibition leads to cellular phenotype correction of DSP-mutated keratinocytes
• Epidermolytic Hyperkeratosis
• Focal acral hyperkeratosis with response to acitretin
• Genetic analysis of seven patients with inherited ichthyosis and Nagashima-type palmoplantar keratoderma
• Genetic basis of a novel rare dominant form of palmoplantar keratoderma
• Hereditary epidermolytic palmoplantar keratosis due to a novel desmoglein-1 mutation: A case report
• Hereditary Punctate Palmoplantar Keratoderma in Three Generations
• HRAS mosaicism in linear palmoplantar keratoderma
• Hyalohyphomycosis (Fusariosis): Atypical Presentation in an Immunocompetent Individual Responding to Itraconazole
• Identification of a founder variant AAGAB c.370C&gt;T, p.Arg124Ter in patients with punctate palmoplantar keratoderma in Southern Denmark
• Identification of a founder variant AAGAB c.370C>T, p.Arg124Ter in patients with punctate palmoplantar keratoderma in Southern Denmark
• Identification of a novel frameshift mutation in cathepsin C gene in a patient with coexisting Papillon-Lefevre syndrome and rheumatoid arthritis
• Invisible palmar needles: thyroid disorder associated spiny keratoderma and the importance of proper light for visualization
• Is punctate palmoplantar keratoderma type 1 associated with malignancy? A systematic review of the literature
• Mal de Meleda
• Microwave Energy for the Treatment of Painful Intractable Plantar Keratosis: A Retrospective Medical Record Review of Nine Patients
• Mutation p.Arg127Pro in the 1A Domain of KRT16 Causes Pachyonychia Congenita in Chinese Patient: A Case Report of PC Associated with Acral Melanoma
• Nagashima-type palmoplantar keratosis associated with Tc17 cells in a patient with rheumatoid arthritis
• NASCI case of the month: desmoplakin cardiomyopathy masquerading as acute myocarditis
• Novel <em>TRPV3</em> loss-of-function mutation in Olmsted syndrome with attenuated phenotype
• Olmsted Syndrome
• Pachyonychia congenita - pathogenesis of pain and approaches to treatment
• Pachyonychia Congenita Project: Advancing Research and Drug Development through Collaboration
• Pachyonychia Congenita: A Research Agenda Leading to New Therapeutic Approaches
• Pachyonychia Congenita: Clinical Features and Future Treatments
• 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 Palmoplantar Lesions Following Vaccination: Answer
• Palmoplantar dermatoses: Diagnostic approach in primary care
• Palmoplantar Keratoderma and Nail Involvement in an Adult
• Palmoplantar Keratoderma Treated with Individualized Homoeopathic Medicine: A Case Report
• Palmoplantar keratoderma, pseudo-ainhum and knuckle pads in an African patient: A case report
• Palmoplantar psoriasis or palmoplantar keratoderma? Successful treatment with brodalumab
• Papillon-Lefevre syndrome in twelve Egyptian patients: Five novel CTSC variants and functional characterization of a missense variant and its effect on splicing
• Paraneoplastic Eczematous Dermatitis With Palmoplantar Keratoderma as an Initial Manifestation of Acute Myeloid Leukemia
• Partial Loss of Function ABCA12 Mutations Generate Reduced Deposition of Glucosyl-Ceramide, Leading to Patchy Ichthyosis and Erythrodermia Resembling Erythrokeratodermia Variabilis et Progressiva (EKVP)
• Pathological mutations reveal the key role of the cytosolic iRhom2 N-terminus for phosphorylation-independent 14-3-3 interaction and ADAM17 binding, stability, and activity
• Pityriasis Rubra Pilaris
• Plantar keratoderma and curly hair as a diagnostic clue of cardiomyopathy risk
• Possible relation of cathepsin C activity and seasonal fluctuation of skin lesions in Papillon-Lefèvre syndrome
• Potential digenic inheritance of SERPINB7 and SERPINA12 variants in Chinese patients with Nagashima-type palmoplantar keratosis
• Prenatal exome sequencing for morphologically normal fetus: Should we be doing it?
• Pseudoainhum and universal alopecia
• Recalcitrant skin ulcers in a patient with Papillon-Lefèvre syndrome: an unusual novel presentation
• Recent developments in the diagnosis, treatment, and management of Papillon-Lefèvre Syndrome
• Role of IL-23 inhibitors including risankizumab and guselkumab in the treatment of pityriasis rubra pilaris
• Self-reported clinical features and treatment effectiveness of Papillon-Lefèvre syndrome patients from five Latin American countries: A cross-sectional online survey study
• SERPINA12-associated palmoplantar keratoderma may be prevalent across different populations
• SERPINB7 Deficiency Increases Legumain Activity and Impairs the Epidermal Barrier in Nagashima-Type Palmoplantar Keratoderma
• Severe atypical juvenile pityriasis rubra pilaris diagnosed in adulthood with a dramatic improvement with ustekinumab
• Severe KIDAR syndrome caused by deletion in the AP1B1 gene: Report of a teenage patient and systematic review of the literature
• Spiny Keratoderma: Clinical and Histopathological Findings in a Series of 3 Cases
• Spontaneous clinical remission of Nagashima-type palmoplantar keratoderma in a patient of Korean descent with a heterozygous SERPINB7 mutation
• The Depressiveness, Quality of Life and NEO-FFI Scale in Patients with Selected Genodermatoses
• The identification of a novel mutation (p.I223fs) in WRN associated with Werner syndrome
• The oral microbiome of a family including Papillon-Lefèvre-syndrome patients and clinically healthy members
• Tiny Vesicles and Papules on the Soles of an Infant
• Transgradient Variant of Mal De Meleda Presenting As Palmoplantar Keratoderma: A Case Report
• Treatment of palmoplantar keratoderma in a patient with ichthyosis with topical tapinarof
• Unexpected Adverse Events of Immune Checkpoint Inhibitors
• Unilateral focal palmoplantar keratoderma associated with a postzygotic variant in PIK3CA and activation of the PI3K/AKT/mTOR pathway
• Unusual Presentation of Aquagenic Palmoplantar Keratoderma with Overlapping Clinical Features with Hereditary Papulotranslucent Acrokeratoderma in a Young Male
• Vohwinkel Syndrome