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About 2,694 results

ALLMedicine™ Optic Atrophy Center

Research & Reviews  1,341 results

Behavioral characterization of a novel Cisd2 mutant mouse.
https://doi.org/10.1016/j.bbr.2021.113187
Behavioural Brain Research; Gaines CH, Snyder AE et. al.

Feb 21st, 2021 - Wolfram syndrome (WFS) is a rare autosomal recessive disorder characterized by diabetes mellitus and insipidus, progressive optic atrophy and sensorineural deafness. An increased incidence of psychiatric disorders has also been reported in WFS pat...

Cytomegalovirus retinitis in a patient of granulomatosis with polyangiitis on long-term...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868283
BMJ Case Reports; Reddy S, Tyagi M et. al.

Feb 5th, 2021 - A 69-year-old male patient presented to the retina clinic with a sudden decrease in vision in his right eye since 1 day. He was a known case of granulomatosis with polyangiitis and was on systemic immunosuppression for the past 3 years. The best-c...

SPOAN syndrome: a novel mutation and new ocular findings; a case report.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809849
BMC Neurology; Bazvand F, Keramatipour M et. al.

Jan 16th, 2021 - To report a novel mutation and new clinical findings in a case with SPOAN syndrome (spastic paraplegia, optic atrophy, neuropathy). Clinical examination, genetic testing and electroretinography were used to study a 2-year-old child who was referre...

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Clinicaltrials.gov  1,349 results

Behavioral characterization of a novel Cisd2 mutant mouse.
https://doi.org/10.1016/j.bbr.2021.113187
Behavioural Brain Research; Gaines CH, Snyder AE et. al.

Feb 21st, 2021 - Wolfram syndrome (WFS) is a rare autosomal recessive disorder characterized by diabetes mellitus and insipidus, progressive optic atrophy and sensorineural deafness. An increased incidence of psychiatric disorders has also been reported in WFS pat...

Cytomegalovirus retinitis in a patient of granulomatosis with polyangiitis on long-term...
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7868283
BMJ Case Reports; Reddy S, Tyagi M et. al.

Feb 5th, 2021 - A 69-year-old male patient presented to the retina clinic with a sudden decrease in vision in his right eye since 1 day. He was a known case of granulomatosis with polyangiitis and was on systemic immunosuppression for the past 3 years. The best-c...

SPOAN syndrome: a novel mutation and new ocular findings; a case report.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7809849
BMC Neurology; Bazvand F, Keramatipour M et. al.

Jan 16th, 2021 - To report a novel mutation and new clinical findings in a case with SPOAN syndrome (spastic paraplegia, optic atrophy, neuropathy). Clinical examination, genetic testing and electroretinography were used to study a 2-year-old child who was referre...

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News  2 results

A 10-Year-Old Boy With Fainting Spells and Seizure Activity
https://reference.medscape.com/viewarticle/884107_6

Sep 24th, 2019 - Question 1 of 2 Which of the following conditions is not associated with congenital LQTS? Your Peers Chose: Congenital sensorineural hearing loss 0% Congenital optic atrophy 0% Syncopal attacks 0% Seizures 0% Sudden cardiac death 0% Important clue...

Case Challenge: A Veteran With Tremor and Impaired Walking
https://www.medscape.com/viewarticle/732033_4

Nov 9th, 2010 - Discussion There are 2 forms of this disease. The classic form usually begins in childhood and manifests with dysarthria, rigidity, spasticity, dystonia, hyperreflexia, Babinski signs, and deterioration of cognitive faculties. Optic atrophy and se...

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Patient Education  2 results see all →