Radiologic presentation of lipoid proteinosis with symmetrical medial temporal lobe calcifications

Lipoid proteinosis is a rare, autosomal-recessive, genetic disorder characterized by multisystem involvement due to intracellular deposition of amorphous hyaline material. The disease is due to a mutation in the extracellular matrix of the protein 1 gene. The skin, mucosa, and central nervous system...

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Bibliographic Details
Main Authors: Subhashree Chandrasekaran, MD (RD) DNB (RD), Murali Nanjundan, MD, Sundari Natarajan, MD, Kannadhasan Ramadhas, MD, DMRD
Format: Article
Language:English
Published: Elsevier 2015-01-01
Series:Radiology Case Reports
Online Access:http://www.sciencedirect.com/science/article/pii/S1930043316300395