Feng-Kun Guo, Christoph Hanhart, Qian Wang, and Qiang Zhao Helmholtz-Institut für Strahlenund Kernphysik and Bethe Center for Theoretical Physics, Universität Bonn, D-53115 Bonn, Germany Institut für Kernphysik and Institute for Advanced Simulation, Forschungszentrum Jülich, D–52425 Jülich, Germany Institute of High Energy Physics and Theoretical Physics Center for Science Facilities, Chinese A...

Richner-Hanhart syndrome (tyrosinemia type II) is a rare autosomal recessive disease associated with high serum tyrosine levels caused by the deficiency of tyrosine aminotransferase enzyme. We report a 15-year-old female patient with complaints of bilateral photophobia and tearing, which started during the infancy period. Biomicroscopic examination revealed bilateral circular corneal opacities ...

Johann Haidenbauer, Christoph Hanhart, Xian-Wei Kang, and Ulf-G. Meißner Institute for Advanced Simulation, Jülich Center for Hadron Physics, and Institut für Kernphysik, Forschungszentrum Jülich, D-52425 Jülich, Germany Helmholtz-Institut für Strahlenund Kernphysik and Bethe Center for Theoretical Physics, Universität Bonn, D-53115 Bonn, Germany (Received 6 July 2015; published 24 September 2015)

Tyrosinemia type II (Richner-Hanhart syndrome) is a rare autosomal recessive disease with deficiency of tyrosine aminotransferase and subsequently increasing level of serum tyrosine. We report the case of a 2-year-old girl who was referred due to bilateral corneal lesions. Slit-lamp examination showed small granular white deposits arranged in a dendritic pattern in the superficial central corne...