Learning objectives
The student will comprehend the physiopathological bases of inherited
metabolic disorders and apply them to the diagnosis and
treatment of the most common inborn conditions.
Prerequisites
Understanding these subjects will require adequate bases of biochemistry,
general pathology and clinical pathology.
Course unit content
Disorders of amino acid metabolism. Disorders of carbohydrate
metabolism. Defects of fatty acid oxydation. Disorders of membrane transport.
Full programme
- - -
Bibliography
Argomenti di Pediatria (M.Vanelli, ed.), Parma 2013 (pp. 197-226). Other
reference material and bibliography/sitography will be provided during
the lessons.
Teaching methods
The course will be held through lectures to Students either in the classroom (“in presenza”) or in synchronous-streaming (“in telepresenza”) on the Teams platform. Therefore, the opportunity of Student/Teacher interaction will be preserved both face to face and remotely, by the simultaneous use of the Teams platform.
Lectures will be supported by slide presentations, which will be available to students on the Elly platform (https://elly2020.medicina.unipr.it/).
The active participation of the students will be stimulated through
discussions of pathophysiology and clinical cases.
Assessment methods and criteria
The fulfillment of didactic objectives will be verified at the level of the whole Course in
Pediatrics through an oral examination that will concern also subjects
treated in this Course.
Other information
- - -
2030 agenda goals for sustainable development
- - -