Abstract
Maple Syrup Urine Disease (MSUD) is an autosomal recessive inborn error of metabolism characterized by decreased enzymatic activity of branched-chain alpha-ketoacid dehydrogenase which leads to an inability to break down branched chain amino acids. It is critical for physicians to make a prompt diagnosis of metabolic disorders to decreased metabolic decompensations and mitigate long-term complications A 33 year old G2 P2 Indian woman with no known family history of MSUD gave …
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
