Hepatolenticular degeneration
A rare autosomal recessive inherited disorder caused by mutations in the ATP7B gene. It is characterized by copper accumulation in the tissues, particularly brain and liver. It results in liver failure, neurologic, and psychotic manifestations.
Disease Alternative Name
Eye Care & Research Centre, Kolkata for About 25 Years
Consultant
Eye Care & Research Centre, Kolkata
MS, DO
Amritsar Eye Hospital
Director
G M C Amritsar
M S ophthalmology
Super Specialist in Reproductive Endocrinology
Ex.central Hospital Dhanbad.1985 ..1993..ex.pathologist .drs Tribedy and Roy Dianostic Lab.kolkata.ex Pathologist.inst of Child Health Kolkata.
Senior Pathologist
School of Tropical Medicine. Kolkata
d c p
Florence Hospital
Sr Consultant Ophthalmologist
POSTED MORE THAN 1600 OPHTHALMIC ARTICLES TILL DATE
20 Years of Teaching To Both UGs & PGs
As Assistant, Associate & Professor
Gandhi Medical College, Dr. NTRUHS
MD Pathology
Kerala University, Utkal University
Mbbs, MD
Aswini Hospital
Villupuram
Tirunelveli Medicalcollege
MBBS
Kothawale Maternity & Surgical Hospital
Assistant Doctor
MUHS Nashik University. Collage- Gulabaroa Patil Homoeopathic Medical College,Miraj
BHMS
Pondicherry Institute of Medical Science
Student
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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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