Healthcare


W8MD Diet | COVID-19 portal | Vitamin D | Vaccine | Keto

WikiMD is the world's largest medical encyclopedia with
13,707 pages, 4,140,686 edits & 38,691,848 views.

Free unbiased diet, health and wellness info!

3 methylcrotonyl coa carboxylase deficiency

From WikiMD's free health, diet & wellness encyclopedia
Jump to navigation Jump to search

3 methylcrotonyl coa carboxylase deficiency - an autosomal recessive inherited disorder caused by mutations in the mccc1 or mccc2 genes. It is characterized by a deficiency in an enzyme that is involved in the metabolism of proteins that contain leucine. Signs and symptoms range from mild to severe and include feeding difficulties, vomiting, diarrhea, developmental delays, lethargy, seizures and coma.

Up to date info

UpToDate

Latest research - 3 methylcrotonyl coa carboxylase deficiency

PubMed
Clinical trials

Source: Data courtesy of the U.S. National Library of Medicine. Since the data might have changed, please query MeSH on 3 methylcrotonyl coa carboxylase deficiency for any updates.

 

3 methylcrotonyl coa carboxylase deficiency is part of WikiMD's free ^articles!

^3 methylcrotonyl coa carboxylase deficiency (article) is provided for informational purposes only. No expressed or implied warranties as to the validity of content.
WikiMD is not a substitute for professional advice. By accessing and using WikiMD you agree to the terms of use.
Templates etc. when imported from Wikipedia, are licensed under CC BY-SA 3.0. See full disclaimers.
W8MD weight loss logo

Ad. Tired of being overweight?. W8MD's physician weight loss program can HELP. Tele medicine available