Lipoid Proteinosis: A Rare Cause of Hoarseness
Author:
Publisher
Elsevier BV
Subject
LPN and LVN,Speech and Hearing,Otorhinolaryngology
Reference32 articles.
1. Otolaryngological manifestations and genetic characteristics of lipoid proteinosis;Xu;Ann Otol Rhinol Laryngol,2010
2. Lipoid proteinosis in an inbred Namaqualand community;Gordon;Lancet,1969
3. Extracellular matrix protein 1 gene (ECM1) mutations in lipoid proteinosis and genotype-phenotype correlation;Hamada;J Invest Dermatol,2003
4. Differentiation-dependent alternative splicing and expression of the extracellular matrix protein 1 gene in human keratinocytes;Smits;J Invest Dermatol,2000
5. Lipoid proteinosis maps to 1q21 and is caused by mutations in the extracellular matrix protein 1 gene (ECM1);Hamada;Hum Mol Genet,2002
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1. Multiple oral submucosal nodules in a young adult;Oral Surgery, Oral Medicine, Oral Pathology and Oral Radiology;2023-10
2. Assessment of dynamic thiol-disulfide homeostasis in patients with lipoid proteinosis (Urbach-Wiethe syndrome);Revista da Associação Médica Brasileira;2022-09
3. Late presentation of laryngeal lipoid proteinosis: a case report and review of the literature;Journal of Surgical Case Reports;2022-08-01
4. Evaluation of choroidal thickness and ocular manifestations in lipoid proteinosis;International Ophthalmology;2022-07-17
5. Pediatric Voice Disorders from the Perspective of Rare Diseases;Journal of Voice;2021-06
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