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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...

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Detalles Bibliográficos
Autores principales: Tabassum, Hera, Mushtaq, Sabha, Amin, Syed Suhail, Adil, Mohammad, Mohtashim, Mohammad, Akhtar, Kafil
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2020
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