Pachydermoperiostosis And An Eyelid Ptosis Associated With Spiky Keratoderma – An Unusual Presentation by S Das, S Chakraborty, NS Sarkar

Subjects: “…Keratoderma…”
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Pachydermoperiostosis And An Eyelid Ptosis Associated With Spiky Keratoderma – An Unusual Presentation by S Das, S Chakraborty, NS Sarkar

Subjects: “…Keratoderma…”
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Isolated plantar punctate porokeratosis: case report by Enas A.S. Attia

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Palmoplantar keratoderma in a middle-aged male by Manisha Siriwardene, BBMedS, MD, Frank Isaacs, MBBS

Subjects: “…palmoplantar keratoderma…”
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A Shared Pathogenesis? Elastic Tissue Degeneration in Two Generations: Co‐Occurrence of Acrokeratoelastoidosis and ARCL1A Cutis Laxa by Sumayyah I Alrefaie, Sarah B. Aljoudi, Houriah Y. Nukaly, Waseem K. Alhawsawi, Asem Shadid, Sultan AlNasser, Jehad Hariri

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Sporadic Progressive Symmetric Erythrokeratoderma: Classical Presentation of a rare Condition by Kompal Agarwal, Sudha Agrawal, Anju Pradhan

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Sporadic Progressive Symmetric Erythrokeratoderma: Classical Presentation of a rare Condition by Kompal Agarwal, Sudha Agrawal, Anju Pradhan

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Geriatric Psoriasis: Evaluation of Clinical Features, Disease Course, and Treatment Modalities of Patients from a Tertiary Care Hospital by Elif Çalışkan, Yusuf Can Edek, Nuray Keskin, Petek Üstün, Esra Adışen

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Increased risk of anxiety and coping strategies in patients with selected genodermatoses with cornification disruption by Magdalena Fryze, Radoslaw Mlak, Aleksandra Kulbaka, Katarzyna Wertheim-Tysarowska, Dariusz Matosiuk, Aldona Pietrzak

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Olmsted Syndrome: A Case Report of Two Brothers by Surendra Singh Bhati, Anmol Bhargava, Pramey Deshpande, Swati Sahu

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A new syndromic case of hearing loss and ectodermal anomalies associated with a recurrent missense variation in GJB6 gene by Badreddine Elmakhzen, Paul Rollier, Clémence Saillard, Benoit Godey, Cédric Le Marechal, Paul Gueguen, Isabelle Fajardy, Sylvie Odent, Laurent Pasquier

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Haim–Munk Syndrome with Cathepsin C Gene Mutation in an Adult from Western India by Sukhdeep Bhatia, Bhushan Darkase, Shekhar Pradhan, Anil Gosavi

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Keratoderma-hypotrichosis-leukonychia Totalis Syndrome: A New Case Report of an Exceptional Entity by Carlos Gutiérrez-Cerrajero, Nerea Gestoso-Uzal, Nelmar Valentina Ortiz-Cabrera, Rogelio González-Sarmiento, Ángela Hernández-Martín

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Carvajal syndrome: a brief overview and clinical case of cardiomyopathy, associated with compound heterozygous mutations of the desmoplakin gene by T. G. Vaikhanskaya, L. N. Sivitskaya, T. V. Kurushko, D. P. Ermakovich, E. V. Zasim, N. G. Danilenko

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Beyond the Common Causes of Palmoplantar Keratoderma: Papillon–Lefevre Syndrome with a Unique Mutation by Sanjanaa Srinivasa, Sumedha Ballal, Preetha Tilak, Savitha Murali, Madhukara Jithendriya

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Immunohistochemical characteristics of inducible nitric oxide synthase and estrogen receptors alpha expression in patients with keratoderma climactericum by H. I. Makurina, S. I. Tertyshnyi, V. H. Siusiuka, O. V. Veretelnyk, O. K. Synakh

Subjects: “…palmoplantar keratoderma…”
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Hereditary Painful Callosities Treated with L5 and S1 Pulsed Radiofrequency, Case Report by Moustafa Moustafa, Kenneth Kuan Boon Keat, Hari Gopal

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Rare Homozygous CTSC Deletion in Siblings with Papillon-Lefevre Syndrome: A Case Report by Fatima AlQaydi, Mohamed Ahmed

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Skin disorders affecting the feet by M. H. Motswaledi

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