Results 1 to 10 of about 11,602 (301)

Acrodermatitis continua of Hallopeau successfully treated with bimekizumab: A case report

SAGE Open Medical Case Reports, 2023
Acrodermatitis continua of Hallopeau is a rare variant of localized pustular psoriasis characterized by the recurrent eruption of sterile pustules involving the distal portions of the fingers and toes that can lead to the destruction of the nail ...
Katrina D Cirone, Fiona E Lovegrove
doaj   +3 more sources

Successful treatment of severe acrodermatitis continua of hallopeau with Bimekizumab: A case report [PDF]

SAGE Open Medical Case Reports
Acrodermatitis continua of Hallopeau is a rare form of pustular psoriasis affecting the acral fingers and toes, characterized by recurrent eruptions of sterile pustules that lead to significant pain and potentially irreversible destruction of the nail ...
Lily Xu, Kaiyang Li, Eric Mutter, Annie Langley   +3 more
doaj   +3 more sources

Successful treatment of acrodermatitis continua of Hallopeau with tildrakizumab: A case report

SAGE Open Medical Case Reports, 2023
Acrodermatitis continua of Hallopeau is a rare, localized variant of pustular psoriasis commonly associated with join disease and severe quality of life impairment.
Alex Nguyen, Kathleen D’Aguanno, Zainab Ridha, Alexander Tsoukas, Elena Netchiporouk   +4 more
doaj   +2 more sources

Palmoplantar pustulosis and acrodermatitis continua of Hallopeau: demographic and clinical comparative study in a large multicentre cohort [PDF]

Journal of the European Academy of Dermatology and Venereology, 2022
Acral pustular disease within the pustular psoriasis/psoriasis‐like spectrum mainly includes palmoplantar pustulosis (PPP) and acrodermatitis continua of Hallopeau (ACH).
Florence Assan, B. Husson, S. Hegazy, Julien Sénéschal, F. Aubin, E. Mahé, D. Jullien, É. Sbidian, M. D’Incan, Curdin Conrad, E. Brenaut, C. Girard, M.‐A. Richard, H. Bachelez, M. Viguier, “Groupe de Recherche sur le Psoriasis” de la Société Française de Dermatologie   +15 more
openalex   +2 more sources

Acquired Zinc Deficiency Mimicking Acrodermatitis Enteropathica in a Breast-Fed Premature Infant

Pediatric Reports, 2021
We present a case of a transient acquired zinc deficiency in a breast-fed, 4-month-old-male prematurely born infant, with acrodermatitis enteropathica-like symptoms such as crusted, eroded, erythemato-squamous eruption in periorificial and acral patterns.
Giovanna D’Amico, Corinne De Laet, Guillaume Smits, Deborah Salik, Guillaume Deprez, Catheline Vilain, Pascale Perlot, Alfredo Vicinanza   +7 more
doaj   +2 more sources

Acrodermatitis continua of Hallopeau: clinical perspectives. [PDF]

Psoriasis, 2019
Acrodermatitis continua of Hallopeau (ACH) is a rare, sterile pustular eruption of one or more digits. The condition presents with tender pustules and underlying erythema on the tip of a digit, more frequently arising on a finger than a toe.
Beck, Kristen M, Bhutani, Tina, Liao, Wilson, Ly, Karen, Smith, Mary Patricia, Thibodeaux, Quinn   +5 more
core   +2 more sources

Acrodermatitis enteropática

Boletín Médico del Hospital Infantil de México, 2017
Introducción: La acrodermatitis enteropática es una enfermedad de baja incidencia que ocurre por deficiencia de zinc; puede ser hereditaria o adquirida. Se caracteriza por dermatitis acral, alopecia, diarrea y problemas de crecimiento.
María Elena Martínez-Bustamante, Rubén Peña-Vélez, Enory Almanza-Miranda, Carlos Andrés Aceves-Barrios, Tonatiuh Vargas-Pastrana, Alfredo Raúl Rodolfo Morayta-Ramírez Corona   +5 more
doaj   +5 more sources

MKLN1 splicing defect in dogs with lethal acrodermatitis [PDF]

PLoS Genetics, 2018
Lethal acrodermatitis (LAD) is a genodermatosis with monogenic autosomal recessive inheritance in Bull Terriers and Miniature Bull Terriers. The LAD phenotype is characterized by poor growth, immune deficiency, and skin lesions, especially at the paws ...
A Grider, A McKenna, AA Koppolu, Anina Bauer, Anne Thomas, B Bai, Barbara Richter, BK Tripathi, Catherine André, Cathryn Mellersh, CF Delto, DR Ledee, E Martoni, Edouard Cadieu, EJ Moynahan, EJ Moynahan, FF Heisler, G Gueron, GA Van der Auwera, H Hasegawa, H Li, H Li, Hannes Lohi, JC Adams, Judith Fischer, KJ Karczewski, L Ding, L Ronnegard, M Lek, M Nassan, M Umeda, M Valiyaveettil, Margret L. Casal, Marjo K. Hytönen, Monika M. Welle, N Kobayashi, N Lakdawala, N Sheth, NA McEwan, NA McEwan, NA McEwan, NA McEwan, Neil A. McEwan, O Francis, P Cingolani, P Debenedittis, Petra Roosje, PF Jezyk, S Küry, S Prag, S Purcell, Sandra Högler, T Kawarai, Tosso Leeb, V Yuzbasiyan-Gurkan, Vidhya Jagannathan, X Li, Y Uchida, YM Park, YS Aulchenko   +59 more
core   +8 more sources

Acrodermatitis Enteropathica: A Case Report

Oman Medical Journal, 2020
Acrodermatitis enteropathica is a rare autosomal recessive disease caused by a genetic mutation leading to zinc deficiency. Clinical manifestation includes skin lesions, diarrhea, and alopecia.
Asma Al Naamani, Tuqa Al Lawati
doaj   +2 more sources

Acrodermatitis Chronica Atrophicans Coexisting with Lichen Sclerosus [PDF]

Przegląd Dermatologiczny
A 38-year-old woman was admitted to the Department of Dermatology due to purple-pinkish macules observed on the thighs and buttocks, which were very firm on palpation.
Julia Nowowiejska-Purpurowicz, Anna Baran, Iwona Flisiak   +2 more
doaj   +2 more sources