Kiliç Birim Günay, Uğur Çağatay, Saday Duman Nagihan, Akçakin Melda
Department of Child and Adolescent Psychiatry, Ankara University Faculty of Medicine, Ankara, Turkey.
Noro Psikiyatr Ars. 2014 Jun;51(2):172-174. doi: 10.4274/npa.y6617. Epub 2014 Jun 1.
Carbonic Anhydrase Type II Deficiency Syndrome (CADS) is a disease with an autosomal recessive inheritance that mainly includes characteristics of osteopetrosis, renal tubular acidosis and cerebral calcification. Pathological fractures, poor vision due to cranial nerve pressure, wide forehead, disproportionate mouth and jaw, physical and mental developmental delay are other features. In this paper, we present the case of a patient who was referred to our department with a diagnosis of CADS and diagnosed with autistic disorder after a psychiatric evaluation. We performed a detailed literature search, however, we did not find any report of co-existence of CADS (osteopetrosis intermediate type) and autistic disorder.
II型碳酸酐酶缺乏综合征(CADS)是一种常染色体隐性遗传疾病,主要特征包括骨硬化、肾小管酸中毒和脑钙化。病理性骨折、因颅神经受压导致视力不佳、额头宽阔、口颌比例失调、身心发育迟缓也是其特征。本文介绍了一名被诊断为CADS并转诊至我科的患者,经精神科评估后被诊断为自闭症谱系障碍。我们进行了详细的文献检索,但未发现任何关于CADS(中间型骨硬化)与自闭症谱系障碍共存的报告。