Abstract
Neurofibromatosis type I (NF-1), the most common neurocutaneous disorder, can be an inherent or spontaneous mutation of the NF-1 gene on chromosome 17q11.2 and encodes neurofibromin proteins. There have only been a few cases reported of NF-1 associated with nephrotic syndrome and the relation rests unclear. Herein, we present a case of NF-1 combined with minimal change disease (MCD).
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 callDisclaimer: 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.
