most common porphyria : acute intermittent porphyria! Autosomal dominant Caused due to deficiency of uroporphyrinogen 1 synthase Clinical features : abdominal and neurological manifestations. No colouration is seen in urine. 😊👍
Bhai from ur videos it is evident that ur putting in a lot of efforts, but how do you manage studying and what makes u stay determined towards your goals?? Btw beard badiyaa haii?!😁
Thanks Bhai! Bas thoda sa discipline,realisation aur fun work balance! Time lagta consistent hone me, but one can manage things if those things really matter!
AIP has port wine urine as mentioned in lippincott and it occurred due to PBG deaminase or hydoxymethylbillase or uroporphobilinogen I synthase deficiency
Porphyria ad acute intermittent ala and porphobilinogen increse abdominal and neurological manifestation no photosensitivity congenital erythropoietic and 4 k symptoms same hote h