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...

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Veröffentlicht in:	Frontiers in pediatrics 2021-04, Vol.9, p.661434, Article 661434
Hauptverfasser:	Di Iorio, Valentina, Mozzillo, Enza, Rosanio, Francesco Maria, Di Candia, Francesca, Genesio, Rita, Testa, Francesco, Iovino, Claudio, Franzese, Adriana, Simonelli, Francesca
Format:	Artikel
Sprache:	eng
Schlagworte:	CISD2 gene Life Sciences & Biomedicine neurodegeneration non-autoimmune diabetes optic atrophy optic neuropathy Pediatrics Science & Technology Wolfram syndrome
Online-Zugang:	Volltext
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