Gyrate atrophy
A rare autosomal recessive inherited disorder caused by mutations in the OAT gene. It is characterized by progressive atrophy of the retina and choroid, leading to loss of vision and blindness.
Recent Cases of Gyrate atrophy
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Top doctors who continously share their opinions on Gyrate atrophy
Florence Hospital
Sr Consultant Ophthalmologist
POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE
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.
S M S Medical College & Hospital
Assistant Professor Ophthalmology
Dr R P Centre, AIIMS,
MD Ophthalmology
Medvarsity Online Limited
Family Medicine
PGIMS New OPD
Optometrists
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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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