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.
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Browse recently discussed Acute intermittent porphyria cases by specialistsNice post.Thanks.In medicine associations often lead to diagnosis.
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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
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Goa Medical College and Hospital
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MS OBSTETRICS AND GYNAECOLOGY
GRH Madurai
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MBBS,MD (Med) ,DM(Neurology),DNB(Neurology), FAAN(Fellow of American Academy of Neurology)
Sikkim Manipul University of Medical and Technology
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