Alsharidi Aynaa, Al-Hamed Mohammad, Alsuwaida Abdulkareem
Department of Medicine (38), College of Medicine, King Saud University, P.O. Box 2925, Riyadh, 11461, Kingdom of Saudi Arabia.
Department of Genetics, King Faisal Specialist and Research Center, Riyadh, Kingdom of Saudi Arabia.
CEN Case Rep. 2016 May;5(1):108-112. doi: 10.1007/s13730-015-0205-y. Epub 2015 Dec 8.
Carbonic anhydrase II (CAII) deficiency is an autosomal recessive disorder characterized by renal tubular acidosis, osteopetrosis, recurrent bone fractures, renal stones, growth failure, and mental retardation. Several cases have been reported in Saudi Arabia with homozygous mutations in CA2 consistent with a high degree of consanguinity. We report a case of carbonic anhydrase II deficiency with short stature, mixed renal tubular acidosis, recurrent bone fractures due to trivial trauma, recurrent renal stones and cerebral calcification. This patient was compound heterozygous for a novel CA2 mutation and a previously reported mutation in Arabs.
碳酸酐酶II(CAII)缺乏症是一种常染色体隐性疾病,其特征为肾小管酸中毒、骨硬化、反复骨折、肾结石、生长发育迟缓及智力障碍。沙特阿拉伯已报道多例CA2基因纯合突变病例,这与高度近亲结婚有关。我们报告1例碳酸酐酶II缺乏症患者,该患者身材矮小,患有混合型肾小管酸中毒,因轻微外伤反复骨折,反复发生肾结石及脑钙化。该患者为一种新的CA2突变与先前报道的阿拉伯人群突变的复合杂合子。