Disorders of tryptophan syndrome
From WikiLectures
Congenital disorders of tryptophan metabolism
- essential AA, including for the production of nicotinic acid and serotonin.
Hartnup's disease[edit | edit source]
- AR hereditary.
- the basis is the abnormal resorption of neutral AMK in the intestine and in the kidneys.
- usually does not cause any clinical symptoms.
- or skin photosensitivity is in the foreground.
Links[edit | edit source]
Source[edit | edit source]
- BENEŠ, Jiří. Studying materials [online]. ©2007. [cit. 2010-04]. <http://www.jirben.wz.cz/>.
References[edit | edit source]
- HRODEK, Otto – VAVŘINEC, Jan, et al. Pediatrie. 1. edition. Praha : Galén, 2002. ISBN 80-7262-178-5.
- ŠAŠINKA, Miroslav – ŠAGÁT, Tibor – KOVÁCS, László, et al. Pediatria. 2. edition. Bratislava : Herba, 2007. ISBN 978-80-89171-49-1.
