Disease: Palmoplantar Keratoderma
- <em>De Novo</em> Mutation in <em>KRT1</em> Leads to Epidermolytic Palmoplantar Keratoderma: from Chinese Traditional Treatment to Prenatal Diagnosis Using Whole-Exome Sequencing-Plus
- <em>DSP</em> c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- A case of Carvajal syndrome presenting with dilated cardiomyopathy
- A case of LSS-associated congenital nuclear cataract with hypotrichosis and literature review
- A Case of Palmoplantar Keratoderma in the Constellation of Connective Tissue Diseases
- A Case Report of Hereditary Palmoplantar Keratoderma with Esophageal Melanosis
- A Japanese case of Vorner-type palmoplantar keratoderma caused by a novel KRT1 variant
- 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 homozygous nonsense mutation in NECTIN4 gene in a Pakistani family with ectodermal dysplasia syndactyly syndrome 1
- 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 telomerase activity and microRNA-21 upregulation identified in a family with 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
- A truncating variant altering the extreme C-terminal region of desmoplakin (DSP) suggests the crucial functional role of the region: a case report study
- Acquired diffuse palmoplantar erythema with keratoderma in Chinese patients with pustular psoriasis: A predictor for IL36 receptor antagonist c.115+6T>C mutation?
- Acrokeratoelastoidosis
- An in-frame 18 bp deletion in linker domain L1 of KRT9 identified in a Japanese patient with epidermolytic palmoplantar keratoderma
- An Institution Based Cross-Sectional Observational Aetiological Study Correlating the Clinico-Pathological Findings in Patients Presenting with Acquired Palmoplantar Keratoderma
- Analysis of the function of ADAM17 in iRhom2 curly-bare and tylosis with esophageal cancer mutant mice
- Aquagenic keratoderma as a consequence of excessive handwashing during the COVID-19 pandemic-A case report
- Aquagenic keratoderma: A rare disease in the COVID age?
- Aquagenic keratoderma: three case reports
- Atypical epidermolytic palmoplantar keratoderma is a minimal phenotypic variant of epidermolytic ichthyosis: A new insight from ultrastructural findings
- 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
- Case report: Area of focus of management of severe pityriasis rubra pilaris by dose optimization of adalimumab biosimilar in combination with acitretin and montelukast
- Cathepsin and cutaneous disorders of cornification and inflammation: their close links
- Cathepsin C role in inflammatory gastroenterological, renal, rheumatic, and pulmonary disorders
- Cathepsin-C mutation in an individual with phenotypic features of Haim-Munk syndrome: a case report
- 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
- De Novo Mutation in KRT1 Leads to Epidermolytic Palmoplantar Keratoderma: from Chinese Traditional Treatment to Prenatal Diagnosis Using Whole-Exome Sequencing-Plus
- Defective cathepsin Z affects EGFR expression and causes autosomal dominant palmoplantar keratoderma
- Desmoplakin mutation underlying autosomal dominant arrhythmogenic cardiomyopathy, palmoplantar keratoderma, and curly hair
- 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
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly 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
- Fossil evidence of tylosis formation in Late Devonian plants
- 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 Punctate Palmoplantar Keratoderma in Three Generations
- HRAS mosaicism in linear palmoplantar keratoderma
- Hyalohyphomycosis (Fusariosis): Atypical Presentation in an Immunocompetent Individual Responding to Itraconazole
- Ichthyosis Follicularis with Alopecia and Photophobia Syndrome with Coexisting Palmoplantar Keratoderma Treated with Acitretin
- Identification of a founder variant AAGAB c.370C>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 compound heterozygous mutation and a homozygous mutation of SLURP1 in Chinese families with Mal de Meleda
- Identification of a novel frameshift mutation in cathepsin C gene in a patient with coexisting Papillon-Lefevre syndrome and rheumatoid arthritis
- Impact of corporate motives for sustainable sourcing: key moderating role of regulatory pressure
- Integration of Phenotype Term Prioritization and Gene Expression Analysis Reveals a Novel Variant in the <em>PERP</em> Gene Associated with Autosomal Recessive Erythrokeratoderma
- 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
- Multiple keratotic projections on the palms and soles
- Nagashima-type palmoplantar keratosis associated with Tc17 cells in a patient with rheumatoid arthritis
- Olmsted Syndrome
- Oral Supplementation with Algal Sulphated Polysaccharide in Subjects with Inflammatory Skin Conditions: A Randomised Double-Blind Placebo-Controlled Trial and Baseline Dietary Differences
- 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
- Painful Palmoplantar Lesions Following Vaccination: Answer
- Palmoplantar Keratoderma and Nail Involvement in an Adult
- 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 partially responsive to treatment with upadacitinib: A case report
- 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
- 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
- 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
- Refining skin lesions classification performance using geometric features of superpixels
- SERPINA12-associated palmoplantar keratoderma may be prevalent across different populations
- Severe KIDAR syndrome caused by deletion in the AP1B1 gene: Report of a teenage patient and systematic review of the literature
- Spiny Keratoderma
- Spontaneous clinical remission of Nagashima-type palmoplantar keratoderma in a patient of Korean descent with a heterozygous SERPINB7 mutation
- Symmetric Palmoplantar Papules With a Keratotic Border
- Tepotinib-Induced Palmoplantar Keratoderma-Like Hand-Foot Skin Reaction
- 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
- Treatment of palmoplantar keratoderma in a patient with ichthyosis with topical tapinarof
- Unexpected Adverse Events of Immune Checkpoint Inhibitors
- Unusual Presentation of Aquagenic Palmoplantar Keratoderma with Overlapping Clinical Features with Hereditary Papulotranslucent Acrokeratoderma in a Young Male
- Vohwinkel Syndrome