Abstract

Background: Congenital disorders of glycosylation (CDGs/INS;) are a rare group of metabolic diseases that have been described in only a few individuals, where phenotypes are continually being updated. Some of these disorders present hemorrhagic or prothrombotic features, but there is not a clear correlation with each individual subtype.

Full Text
Paper version not known

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

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.