Clinical and histopathological response to acitretin therapy in lipoid proteinosis
Author:
Publisher
Informa UK Limited
Subject
Dermatology
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
Reference18 articles.
1. Lipoidosis cutis et mucosae
2. Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1)
3. The molecular basis of lipoid proteinosis: mutations in extracellular matrix protein 1
4. Lipoid Proteinosis: Report of Four Siblings and Brief Review of the Literature
5. Lipoid proteinosis: a case series from Istanbul
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1. A founder deletion in ECM1 of 1163 bp causes lipoid proteinosis in the southeast region of Turkiye;American Journal of Medical Genetics Part A;2024-06-06
2. Advances in treatment for lipoid proteinosis (Urbach–Wiethe disease): a case report and systematic review;Clinical and Experimental Dermatology;2024-02-03
3. Cranial magnetic resonance imaging findings and their relationship with neuropsychiatric findings in adult patients with lipoid proteinosis;Gulhane Medical Journal;2022-03-07
4. Successful use of acitretin in an indian child with lipoid proteinosis;Indian Journal of Paediatric Dermatology;2022
5. Lipoid proteinosis;Mucosa;2021-06-30
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