A Tajana

We don’t have enough information about this author to calculate their statistics. If you think this is an error let us know.
Learn More
An 8-year-old boy with galactose-1-phosphate uridyl transferase (GALT) deficiency presented with hypotonia, muscle hypotrophy, hepatomegaly, bilateral cataract and mild mental retardation. Two brothers showed a GALT activity consistent with a homozygotic condition and both parents were found to be heterozygotes for this defect. Histological and(More)
Although haemorrhoids have been known for centuries, there is still some controversy on the subject. In addition little attention has so far been paid to their appearance in young people. The incidence and aetiopathogenesis of the condition and the correct therapeutic approach are discussed on the basis of personal experience, clinical research and recent(More)
  • 1