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2
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Evaluation of carbonic anhydrase isozymes in disorders involving osteopetrosis and/or renal tubular acidosis.在涉及骨质石化症和/或肾小管酸中毒的病症中对碳酸酐酶同工酶的评估。
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Carbonic anhydrase II deficiency in 12 families with the autosomal recessive syndrome of osteopetrosis with renal tubular acidosis and cerebral calcification.12个患有常染色体隐性遗传的骨硬化症伴肾小管酸中毒和脑钙化综合征家庭中的碳酸酐酶II缺乏症
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Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal tubular acidosis and brain calcification): novel mutations in CA2 identified by direct sequencing expand the opportunity for genotype-phenotype correlation.碳酸酐酶II缺乏综合征(伴有肾小管酸中毒和脑钙化的骨质石化症):通过直接测序鉴定出的CA2新突变增加了基因型与表型相关性研究的机会。
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本文引用的文献

1
Osteopetrosis.骨质石化症
Orphanet J Rare Dis. 2009 Feb 20;4:5. doi: 10.1186/1750-1172-4-5.
2
Carbonic anhydrase II deficiency syndrome (osteopetrosis with renal tubular acidosis and brain calcification): novel mutations in CA2 identified by direct sequencing expand the opportunity for genotype-phenotype correlation.碳酸酐酶II缺乏综合征(伴有肾小管酸中毒和脑钙化的骨质石化症):通过直接测序鉴定出的CA2新突变增加了基因型与表型相关性研究的机会。
Hum Mutat. 2004 Sep;24(3):272. doi: 10.1002/humu.9266.
3
Molecular mechanism of kNBC1-carbonic anhydrase II interaction in proximal tubule cells.近端小管细胞中kNBC1与碳酸酐酶II相互作用的分子机制。
J Physiol. 2004 Aug 15;559(Pt 1):55-65. doi: 10.1113/jphysiol.2004.065110. Epub 2004 Jun 24.
4
The genetics of autism.自闭症的遗传学
Pediatrics. 2004 May;113(5):e472-86. doi: 10.1542/peds.113.5.e472.
5
Developmental expression of carbonic anhydrase-related proteins VIII, X, and XI in the human brain.碳酸酐酶相关蛋白VIII、X和XI在人脑中的发育表达。
Neuroscience. 2002;112(1):93-9. doi: 10.1016/s0306-4522(02)00066-0.
6
Long-term follow up of carbonic anhydrase II deficiency syndrome.
Saudi Med J. 2002 Jan;23(1):25-9.
7
Carbonic anhydrase gating of attention: memory therapy and enhancement.
Trends Pharmacol Sci. 2002 Feb;23(2):83-9. doi: 10.1016/s0165-6147(02)01899-0.
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Genetics of autism.自闭症的遗传学
Child Adolesc Psychiatr Clin N Am. 2001 Apr;10(2):333-50.
9
Bone marrow transplantation corrects osteopetrosis in the carbonic anhydrase II deficiency syndrome.骨髓移植可纠正碳酸酐酶 II 缺乏综合征中的骨质石化症。
Blood. 2001 Apr 1;97(7):1947-50. doi: 10.1182/blood.v97.7.1947.
10
Marble brain syndrome: osteopetrosis, renal acidosis and calcification of the brain.
Neuroradiology. 1998 Oct;40(10):662-3. doi: 10.1007/s002340050660.

一例伴有孤独症谱系障碍的2型碳酸酐酶缺乏综合征病例。

A Case of Carbonic Anhydrase Type 2 Deficiency Syndrome with Autistic Disorder.

作者信息

Kiliç Birim Günay, Uğur Çağatay, Saday Duman Nagihan, Akçakin Melda

机构信息

Department of Child and Adolescent Psychiatry, Ankara University Faculty of Medicine, Ankara, Turkey.

出版信息

Noro Psikiyatr Ars. 2014 Jun;51(2):172-174. doi: 10.4274/npa.y6617. Epub 2014 Jun 1.

DOI:10.4274/npa.y6617
PMID:28360619
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5353094/
Abstract

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.

摘要

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。