Optic Disc Drusen in a Child Diagnosed with Alport Syndrome—Case Report

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Author(s)    

Adamu Sambo¹, Mona Aslam², Syam Padmanabha²

Affiliation(s)

¹University Hospital of Leicester, Leicester, UK.
²Peterborough City Hospital, Peterborough, UK.

ABSTRACT

Optic disc drusen are eye abnormalities characterised by calcific degeneration affecting some axons of the optic nerve. Alport syndrome is a collagen IV related nephropathy with well-described pathognomonic ocular features. We present the case of a child who following series of investigations was found to have bilateral optic disc drusen, and eventually a further diagnosis of Alport syndrome confirmed. Literature is clear on the underlined aetiology responsible for both renal and extra renal abnormalities of Alport syndrome, which is not related to development of optic disc drusen. The case described makes it pertinent that not only the associated eye signs of Alport syndrome are monitored, but also early detection of other possible co-existing diseases that may influence outcomes.

KEYWORDS

Alport Syndrome, Optic Disc Drusen, Pseudopapilloedema

Cite this paper

Sambo, A. , Aslam, M. and Padmanabha, S. (2014) Optic Disc Drusen in a Child Diagnosed with Alport Syndrome—Case Report. Open Journal of Nephrology, 4, 142-145. doi: 10.4236/ojneph.2014.44020. 

 

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