Protoporphyria
A rare congenital metabolic disorder characterized by an inborn error of porphyrin-heme biosynthesis. It is caused by deficiency of the enzyme ferrochelatase. Signs and symptoms include painful cutaneous photosensitivity leading to blistering and scarring of the exposed skin areas, erythrodontia, red discoloration of urine, hemolytic anemia, and splenomegaly.
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Capital Hospital
EX HOD CARDIOLOGY & HOD MEDICINE
M.K.C.G MEDICAL COLLEGE BERHAMPUR, S.C.B MEDICAL COLLEGE CUTTACK , SPECIALLY TRAINED IN CARDIOLOGY IN DR B. NANAVATI HOSPITAL MUMBAI , & DR SUNDARLAL JAIN HOSPITAL NEW DELHI.
M.B.B.S ( GOLD MEDALIST) , M.D. MEDICINE & CARDIOLOGIST SR DIABETOLOGY
PGIMER, Chandigarh
MD
GSVM Medical College
MBBS
GRH Madurai
Mbbs
Madurai Medical College
MBBS
S.A.S.Hi-Tech Hospital Bhopal
Rmo
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