Acute intermittent porphyria
A genetic metabolic disorder inherited in an autosomal dominant pattern. It is caused by a deficiency of the enzyme porphobilinogen deaminase, which is involved in heme biosynthesis. Signs and symptoms include nausea, vomiting, severe abdominal pain and distension, urinary retention, port-wine urine discoloration, hypertension, tachycardia, muscle weakness, loss of sensation, anxiety, depression, and arm, leg and back pain.
Disease Alternative Name
Medical Component OfHCM
Remained Incharge Medical Officer with Hon'Ble C.M of J and K for More Than 20 Years from Jan 2000 To October 2020
Govt. Medical College, Jammu
M.S (General Surgery )
Goa Medical College and Hospital
Senior Resident
Goa Medical College , Bambolim Goa
MS OBSTETRICS AND GYNAECOLOGY
GRH Madurai
Mbbs
Madurai Medical College
MBBS
Kerala Institute of Medical Sciences
Professor and Senior Consultant Neurology
Medical College Thiruvananthapuram
MBBS,MD (Med) ,DM(Neurology),DNB(Neurology), FAAN(Fellow of American Academy of Neurology)
Sikkim Manipul University of Medical and Technology
Bsc Medical Bio Chemistry
Rainbow New Life Hospital
Medical Officer
Apex Institute of Medical Sciences
BIM&T
RGKMCH
Student
RGKMCH
MBBS
PGIMER, Chandigarh
MD
SBMCH
M.D. DM
Madras Medical College Formerly Professor HOD Pediatric Neurology
DM Neurology MD Pediatrics DCH
NRS Medical College
MBBS Student
NRS Medical College
MBBS
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