Pigmentary maculopathy in a patient with Wolfram syndrome

scientific article published in February 2006

Pigmentary maculopathy in a patient with Wolfram syndrome is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1016/S0008-4182(06)80064-5
P698PubMed publication ID16462870

P2093author name stringUday R Desai
Mandeep S Dhalla
Daniel S Zuckerbrod
P2860cites workDeletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).Q33893745
Juvenile diabetes mellitus, optic atrophy, hearing loss, diabetes insipidus, atonia of the urinary tract and bladder, and other abnormalities (Wolfram syndrome). A review of 88 cases from the literature with personal observations on 3 new patientsQ38793418
Ophthalmologic findings in fifteen patients with Wolfram syndromeQ44001399
Juvenile diabetes mellitus, optic atrophy, sensory nerve deafness, and diabetes insipidus--a syndrome.Q50625177
Optic atrophy in Wolfram (DIDMOAD) syndromeQ74427625
P433issue1
P304page(s)38-40
P577publication date2006-02-01
P1433published inCanadian Journal of OphthalmologyQ15749645
P1476titlePigmentary maculopathy in a patient with Wolfram syndrome
P478volume41

Reverse relations

cites work (P2860)
Q37458535Expression of the diabetes risk gene wolframin (WFS1) in the human retina
Q88724954Genetic and clinical aspects of Wolfram syndrome 1, a severe neurodegenerative disease
Q38635262Retinal thickness as a marker of disease progression in longitudinal observation of patients with Wolfram syndrome
Q38567104The Eye on Mitochondrial Disorders.
Q92131965Wolfram syndrome, a rare neurodegenerative disease: from pathogenesis to future treatment perspectives
Q37656500Wolfram syndrome: important implications for pediatricians and pediatric endocrinologists