Case Report: Ophthalmologic Evaluation Over a Long Follow-Up Time in a Patient With Wolfram Syndrome Type 2: Slowly Progressive Optic Neuropathy as a Possible Clinical Finding

Case Report: Ophthalmologic Evaluation Over a Long Follow-Up Time in a Patient With Wolfram Syndrome Type 2: Slowly Progressive Optic Neuropathy as a Possible Clinical Finding

Wolfram syndrome (WFS) is a rare autosomal recessive neurodegenerative disease whose diagnosis requires diabetes mellitus and optic atrophy (OA). WFS includes a wide spectrum of other possible complications such as diabetes insipidus, sensorineural deafness, urinary tract problems, neurological and...

Full description

Bibliographic Details
Main Authors: Valentina Di Iorio, Enza Mozzillo, Francesco Maria Rosanio, Francesca Di Candia, Rita Genesio, Francesco Testa, Claudio Iovino, Adriana Franzese, Francesca Simonelli
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-04-01
Series:Frontiers in Pediatrics
Subjects:
CISD2 gene
optic atrophy
optic neuropathy
neurodegeneration
non-autoimmune diabetes
Wolfram syndrome
Online Access:https://www.frontiersin.org/articles/10.3389/fped.2021.661434/full

Internet

https://www.frontiersin.org/articles/10.3389/fped.2021.661434/full

Similar Items