Cargando…

Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases

Detalles Bibliográficos
Autores principales:	MAZEREEUW-HAUTIER, Juliette, BOURRAT, Emmanuelle, TOURNIER, Emilie, BATTISTELLA, Maxime, BERNABEU-WITTEL, José, BARBAROT, Sébastien, HERNANDEZ-MARTIN, Angela
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Society for Publication of Acta Dermato-Venereologica 2021
Materias:	Short Communication
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9366501/ https://www.ncbi.nlm.nih.gov/pubmed/33313938 http://dx.doi.org/10.2340/00015555-3720

Ejemplares similares

Alitretinoin reduces erythema in inherited ichthyosis
por: Onnis, Giuliana, et al.
Publicado: (2018)

Prevalence of inherited ichthyosis in France: a study using capture-recapture method
por: Dreyfus, Isabelle, et al.
Publicado: (2014)

Identification of Mutations in SDR9C7 in Three Patients with Autosomal Recessive Congenital Ichthyosis
por: MAZEREEUW-HAUTIER, Juliette, et al.
Publicado: (2020)

New developments in the molecular treatment of ichthyosis: review of the literature
por: Joosten, M. D. W., et al.
Publicado: (2022)

Fatal Neonatal DOLK-CDG as a Rare Form of Syndromic Ichthyosis
por: Komlosi, Katalin, et al.
Publicado: (2021)

Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome
por: ALBLUWI, Shatha, et al.
Publicado: (2020)

Prevalence and risk factors of vitamin D deficiency in inherited ichthyosis: A French prospective observational study performed in a reference center
por: Frascari, Flora, et al.
Publicado: (2014)

TOPICOP©: A New Scale Evaluating Topical Corticosteroid Phobia among Atopic Dermatitis Outpatients and Their Parents
por: Moret, Leïla, et al.
Publicado: (2013)

Congenital heart disease in harlequin ichthyosis: Case series
por: Verma, Bhupendra, et al.
Publicado: (2019)

Novel CLDN1 Deletion Associated with Ichthyosis, Sclerosing Cholangitis and Acquired Alopecia
por: ALSAFRI, Maleha S., et al.
Publicado: (2020)

Corneal ulcer secondary to ectropion in lamellar Ichthyosis: A rare congenital disorder
por: Bhedasgaonkar, Sayali S., et al.
Publicado: (2020)

A novel combination of mutations leading to congenital ichthyosis and ichthyosis vulgaris
por: Shearer, Zackary, et al.
Publicado: (2023)

Congenital bilateral ectropion in lamellar ichthyosis
por: Chakraborti, Chandana, et al.
Publicado: (2011)

Azathioprine Hypersensitivity Syndrome: Two Cases of Febrile Neutrophilic Dermatosis Induced by Azathioprine
por: Aleissa, Majed, et al.
Publicado: (2017)

Current Strategies for the Gene Therapy of Autosomal Recessive Congenital Ichthyosis and Other Types of Inherited Ichthyosis
por: Chulpanova, Daria S., et al.
Publicado: (2022)

Quality of life in Swedish children with congenital ichthyosis
por: Gånemo, Agneta
Publicado: (2010)

Spontaneous subconjunctival abscess in congenital lamellar ichthyosis
por: Bubanale, Shivanand C, et al.
Publicado: (2018)

Ulceration of the Scalp
por: Mackellar, E. D.
Publicado: (1880)

Becker’s Naevus Syndrome with Breast Aplasia Due to Postzygotic Mutation of ACTB
por: RAMSPACHER, Jeanne, et al.
Publicado: (2022)

Mutational Spectrum of the ABCA12 Gene and Genotype–Phenotype Correlation in a Cohort of 64 Patients with Autosomal Recessive Congenital Ichthyosis
por: Hotz, Alrun, et al.
Publicado: (2023)

L’érythème en lunettes, un signe commun au syndrome inflammatoire multisystémique pédiatrique (PIMS) et à la maladie de Kawasaki
por: Piroth, M., et al.
Publicado: (2022)

Congenital Ichthyosis: A Case Treated Successfully With Acitretin
por: Gulasi, Selvi
Publicado: (2016)

Prenatal diagnosis of congenital harlequin ichthyosis with fetal MRI
por: Kale, Kiran A, et al.
Publicado: (2019)

An Intractable Ulcer on the Scalp
por: Maplestone, P. A., et al.
Publicado: (1935)

Ichthyosis
por: Young, A. A.
Publicado: (1910)

Keratitis-Ichthyosis-Deafness syndrome: A rare congenital disorder
por: Shanker, Vinay, et al.
Publicado: (2012)

Recognition and management of congenital ichthyosis in a low-income setting
por: Saso, Anja, et al.
Publicado: (2019)

Lipedematous Scalp with Varied Presentations: A Case Series of Four Patients
por: Sahu, Priyadarshini, et al.
Publicado: (2019)

An enlarging, ulcerated scalp nodule
por: Afifi, Ladan, et al.
Publicado: (2018)

A large scalp ulceration
por: Guerra, Karla, et al.
Publicado: (2021)

Oral epigallocatechin-3-gallate for treatment of dystrophic epidermolysis bullosa: a multicentre, randomized, crossover, double-blind, placebo-controlled clinical trial
por: Chiaverini, Christine, et al.
Publicado: (2016)

Segmental schwannomatosis: characteristics in 12 patients
por: Alaidarous, Abdulqader, et al.
Publicado: (2019)

Targeted regions sequencing identified four novel PNPLA1 mutations in two Chinese families with autosomal recessive congenital ichthyosis
por: Li, Liangshan, et al.
Publicado: (2019)

A Novel ABCA12 Mutation in Two Families with Congenital Ichthyosis
por: Walsh, D. M., et al.
Publicado: (2012)

Mutations in CERS3 Cause Autosomal Recessive Congenital Ichthyosis in Humans
por: Radner, Franz P. W., et al.
Publicado: (2013)

Isotretinoin Treatment for Autosomal Recessive Congenital Ichthyosis in a Golden Retriever
por: Petak, Ana, et al.
Publicado: (2022)

PNPLA1-Mediated Acylceramide Biosynthesis and Autosomal Recessive Congenital Ichthyosis
por: Zeng, Fansi, et al.
Publicado: (2022)

Ichthyosis hystrix
por: Nayak, Surajit, et al.
Publicado: (2013)

Heredity in Ichthyosis
por: Kothari, B. M.
Publicado: (1936)

Erosive pustular dermatosis of the scalp associated with lamellar ichthyosis successfully treated with dehydrated human amnion/chorion membrane allograft
por: Kempton, Darren M., et al.
Publicado: (2018)

Cannot write session to /tmp/vufind_sessions/sess_qt11piao5ofos8t98evlocjc7k