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...
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 |
Similar Items
-
Bilateral selective amygdala calcifications: lipoid proteinosis
by: C Yilmaz, et al.
Published: (2013-07-01) -
Lipoid proteinosis
by: Mukhija Pooja, et al.
Published: (2006-01-01) -
Lipoid proteinosis
by: Sen Sumit, et al.
Published: (2006-01-01) -
Lipoidoproteinose Lipoid proteinosis
by: Sara Nader Marta, et al.
Published: (2008-09-01) -
Lipoid proteinosis in two siblings
by: Behera Samira Kumar, et al.
Published: (2006-01-01)