ePoster - Other

• 102 • Establishing the first genodermatoses registry in Canada: the SickKids’ experience > Y. Yiming WANG (Toronto) • 103 • Mandibuloacral dysplasia type A (MADA) – Novel gadget designed to provide mobility of the child > A. Arun INAMADAR (Vijayapura) • 104 • Three Stepwise pH Zonation in the Stratum Corneum for Homeostatic Maintenance of the Skin > K. Keitaro FUKUDA (Yokohama, Kanagawa) • 108 • A Systematic Review on Postzygotic Mosaicism in Epidermal Nevi: From Variant to Phenotype > A. Aude BEYENS (Ghent) • 109 • Pregnancy-related issues in rare and low-prevalence dermatological diseases: The point of view of Healthcare Professionals in Europe > M-C. Marie-Claude BOITEUX (Bons En Chablais) • 110 • Mycoplasma-Induced Rash and Mucositis > E. Edita MARVANOVA (Brno) • 111 • Porphyria cutanea tarda mimicking pansclerotic morphea > E. Edita MARVANOVA (Brno) • 133 • Exploring the Impacts of a Community-based Storytelling Intervention on the Mental Health, Wellbeing and Empowerment of Persons Affected by Leprosy. > L. Lucy MCKANE (Liverpool) • 142 • MAP2K1 mosaicism – a new cause of phakomatosis pigmentovascularis spilorosea > H. Helene AUBERT (Nantes) • 152 • Atrophic skin, lipodystrophy and acro-facial anomalies revealing a rare pediatric progeroid disorder in a dermatology setting > G. Giulia PASCOLINI (Rome) • 165 • Spontaneous resolution of congenital melanocytic naevi on the scalp > N. Nicole KNÖPFEL (Zurich) • 174 • Refractory early-onset pruritic dermatosis with pustules, follicle hyperkeratosis and superinfections > M. Maria Elena GIMENO RIBES (Tres Cantos) • 175 • Perforating Sarcoidosis of the Scalp: A Rare Clinical Presentation > D. Diego LÓPEZ DA MOTTA (Montevideo) • 176 • Progressive Symmetric Erythrokeratodermia due to gain of function mutation in TRPM4 > J. Josephine HOFMANN (Munich) • 183 • Synchronous Remote Therapeutic Education for Patients with Hereditary Ichthyosis: Feasibility Study of a Dedicated Web Application > I. Isabelle DREYFUS • 184 • KRT1-Related Epidermolytic Ichthyosis with Palmoplantar and Flexural Hyperkeratosis: A Rare Localized Presentation > J. Juliette MAZEREEUW-HAUTIER (Toulouse) • 185 • Neonatal compartment syndrome : a rare and not well known syndrome > N. Naia OILLARBURU (Toulouse) • 24 • Beyond the Expected: Dual Diagnosis of Neurofibromatosis type I and Steatocystoma Multiplex > K. Kakha BREGVADZE (Tbilisi) • 53 • Clinical variability and Genetic Spectrum of POGLUT1-Related Diseases > M. Margaux MAZEAS (Paris) • 67 • A Descriptive Study of the Clinical and Dermoscopic Attributes of Darier Disease > N. Nisim ASAYAG (Afula) • 75 • Inter-rater agreement of the Krengel classification as a physician and patient self-classification tool for congenital melanocytic naevi > N. Nienke DEN HERTOG (Amsterdam) • 86 • Dercum disease: Clinical outcomes and a novel therapeutic approach with GLP-1 receptor agonists from a single-center case series > A. Alessandro MAGNATTA (Florence)