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Lipoid Proteinosis with Esotropia: Report of a Rare Case and Dermoscopic Findings
Lipoid proteinosis (LP) is a rare progressive autosomal recessive disorder caused by mutations in the extracellular matrix protein 1 gene present on chromosome 1q21. It is characterized by infiltration of hyaline material into the skin, mucosae, and internal organs. Patients present with a classical...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6986117/ https://www.ncbi.nlm.nih.gov/pubmed/32029942 http://dx.doi.org/10.4103/ijd.IJD_523_18 |