Assessment
Questionnaire
See what questions
a doctor would ask.
Alpha-mannosidase deficiency: An inborn error of metabolism marked by a defect in the lysosomal isoform of ALPHA-MANNOSIDASE activity that results in lysosomal accumulation of mannose-rich intermediate metabolites. Virtually all patients have psychomotor retardation, facial coarsening, and some degree of dysostosis multiplex. It is thought to be an autosomal recessive disorder.
Source: Diseases Database
These medical condition or symptom topics may be relevant to medical information for Alpha-mannosidase deficiency:
Source: Diseases Database
Source: Diseases Database
Search to find out more about Alpha-mannosidase deficiency:
|
Tools & Services:
Medical Articles:
Search Specialists by State and City
By using this site you agree to our Terms of Use. Information provided on this site is for informational purposes only; it is not intended as a substitute for advice from your own medical team. The information on this site is not to be used for diagnosing or treating any health concerns you may have - please contact your physician or health care professional for all your medical needs. Please see our Terms of Use.
Copyright © 2011 Health Grades Inc. All rights reserved. Last Update: 7 May, 2013 (1:16)