https://i.ytimg.com/vi/MdwPF6ox5FU/mqdefault.jpg
02/24/2015 06:32:24
Presentation by Dr. Ira Shah on Metabolic Liver Diseases
Incidence cause of pediatric liver transplants common cause of metabolic liver disease in India.
Our experience in metabolic liver disease. It's types of disease why liver damage occurs, which are metabolic liver disease
Pathological manifestation, alpha 1 Antitrypsin deficiency treatment, cystic fibrosis case, disorders of bile acid synthesis, Wilson's disease, hepatic presentation(in absence of neurological manifestation)diagnosis, hereditary fructose intolerance, what is Galactosemia, glycogen storage disease, what is the diagnosis, investigations tyrosinemia, presentation of acute liver failure, chronic liver disease, hcc, renal tubular dysfunction, episodic porphyria -like neurological episodes caused by succinyl acetone inhibiting the metabolism of aminolevulinic acid, other metabolic disorders in which the liver has the enzyme defect mitochondrial disorders urea cycle defects, methylmalonic & propionic acidemia, maple syrup urine disease, primary hyperoxaluria, criggler najjer syndrome, Niemann pick type c, porphyria, lysosomal storage diseases.
-~-~~-~~~-~~-~-
For more info visit our WEBSITE Pediatric Oncall: https://www.pediatriconcall.com/
SUBSCRIBE to Pediatric Oncall for more such videos: https://www.youtube.com/pediatriconcall
FOLLOW us on social media pages for updates and regular case discussions:
Facebook: www.facebook.com/PediatricOncall/
Instagram: https://www.instagram.com/pediatriconcall
Twitter: https://twitter.com/pediatriconcall
-~-~~-~~~-~~-~-
Also check out Dr. Ira Shah's talk on Introduction to Mantoux test | Pediatric Oncall
https://youtu.be/CzD9x-yNChk
Dr Ira Shah : Metabolic Liver Diseases
Description
Presentation by Dr. Ira Shah on Metabolic Liver Diseases
Incidence cause of pediatric liver transplants common cause of metabolic liver disease in India.
Our experience in metabolic liver disease. It's types of disease why liver damage occurs, which are metabolic liver disease
Pathological manifestation, alpha 1 Antitrypsin deficiency treatment, cystic fibrosis case, disorders of bile acid synthesis, Wilson's disease, hepatic presentation(in absence of neurological manifestation)diagnosis, hereditary fructose intolerance, what is Galactosemia, glycogen storage disease, what is the diagnosis, investigations tyrosinemia, presentation of acute liver failure, chronic liver disease, hcc, renal tubular dysfunction, episodic porphyria -like neurological episodes caused by succinyl acetone inhibiting the metabolism of aminolevulinic acid, other metabolic disorders in which the liver has the enzyme defect mitochondrial disorders urea cycle defects, methylmalonic & propionic acidemia, maple syrup urine disease, primary hyperoxaluria, criggler najjer syndrome, Niemann pick type c, porphyria, lysosomal storage diseases.
-~-~~-~~~-~~-~-
For more info visit our WEBSITE Pediatric Oncall: https://www.pediatriconcall.com/
SUBSCRIBE to Pediatric Oncall for more such videos: https://www.youtube.com/pediatriconcall
FOLLOW us on social media pages for updates and regular case discussions:
Facebook: www.facebook.com/PediatricOncall/
Instagram: https://www.instagram.com/pediatriconcall
Twitter: https://twitter.com/pediatriconcall
-~-~~-~~~-~~-~-
Also check out Dr. Ira Shah's talk on Introduction to Mantoux test | Pediatric Oncall
https://youtu.be/CzD9x-yNChk