Retinitis pigmentosa
A rare inherited retinal dystrophy disorder characterized by spots of black bone-spicule pigmentation of the retinal pigment epithelium. It is manifested with decreased vision in low light or in the night, followed by decreased peripheral vision, and, eventual decreased central vision. It may lead to blindness.
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4. Digenic
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To me it looks like a healed toxoplasmic retinochoroiditis with consecutive optic atrophy
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Salmon Patch appearance
Recent Cases of Retinitis pigmentosa
Browse recently discussed Retinitis pigmentosa cases by specialists33 Views
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RETINITIS PIGMENTOSA (RP) This is pigmentary RP . Retinal dystrophies are hereditary retinal diseases without any known cause in which ultimately there is premature cell death.
Top Cases of Retinitis pigmentosa
Selected by editors, top cases are known for unique problem or best solutionTop Retinitis pigmentosa Doctors on Curofy
Top doctors who continously share their opinions on Retinitis pigmentosaFlorence Hospital
Sr Consultant Ophthalmologist
POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE
Amritsar Eye Hospital
Director
G M C Amritsar
M S ophthalmology
Eye Care & Research Centre, Kolkata for About 25 Years
Consultant
Eye Care & Research Centre, Kolkata
MS, DO
Divyajyot Eye Hospital.
M.S. (Ophthalmology ).
Government Medical College, Surat.
M.S (Ophthalmology ); D.O; M.B.B.S.
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A 57 yrs old male patient c/o sudden vision loss/left side weakness/agitated/fever bodyache *Chief Complaints* Sudden vision loss Left side weakness Unable to walk Agitated urge to pee/poop but nothing comes out when he go Bodyache *History* CVA with left hemisphere 3 yrs back K/c/o HTN/DM *Vitals* BP 150/80 Pulse 68 Spo2 98 *Physical Examination* B/L Pupils dilated Left side weakness Chest -B/L clear P/A- soft no any tenderness or distension CNS -Alert and aware Genitals -Normal *Investigations* Attached *Diagnosis* CVA with HTN/DM ?TIA/Retinal detachment *Management* Medically conservative Kindly suggest
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