Sandberg H O
Acta Ophthalmol (Copenh). 1975 Nov;53(5):760-4. doi: 10.1111/j.1755-3768.1975.tb01192.x.
A case of tyrosinosis due to lack of soluble tyrosine aminotransferase is described. The first clinical sign of this disorder may be bilateral keratopathy. Treatment is diet with restriction of phenylalanine and tyrosine. The disorder is rare and must be differentiated from other conditions of tyrosinosis.
本文描述了一例因缺乏可溶性酪氨酸转氨酶导致的酪氨酸血症病例。这种疾病的首个临床症状可能是双侧角膜病变。治疗方法是采用限制苯丙氨酸和酪氨酸的饮食。该疾病较为罕见,必须与其他酪氨酸血症情况相鉴别。