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Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?

作者信息

Revesz T, Fletcher S, al-Gazali L I, DeBuse P

机构信息

Department of Paediatrics, Faculty of Medicine and Health Sciences, UAE University, Al Ain, United Arab Emirates.

出版信息

J Med Genet. 1992 Sep;29(9):673-5. doi: 10.1136/jmg.29.9.673.

DOI:10.1136/jmg.29.9.673
PMID:1404302
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1016105/
Abstract

A male infant was found to have bilateral exudative retinopathy at 6 months of age. A month later severe aplastic anaemia was diagnosed, eventually leading to the infant's death. Additional features of this seemingly new syndrome were intrauterine growth retardation, fine sparse hair, fine reticulate skin pigmentation, ataxia because of cerebellar hypoplasia, cerebral calcifications, extensor hypertonia, and progressive psychomotor retardation.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e098/1016105/2f24c6fc387e/jmedgene00023-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e098/1016105/346cb80e9a23/jmedgene00023-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e098/1016105/2f24c6fc387e/jmedgene00023-0076-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e098/1016105/346cb80e9a23/jmedgene00023-0075-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e098/1016105/2f24c6fc387e/jmedgene00023-0076-a.jpg

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本文引用的文献

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Dyskeratosis congenita with hypoplastic anemia: a stem cell defect.
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2
A familial syndrome with coats' reaction retinal angiomas, hair and nail defects and intracranial calcification.
Eye (Lond). 1988;2 ( Pt 3):297-303. doi: 10.1038/eye.1988.56.
3
Dyskeratosis congenita.先天性角化不良
J Med Genet. 1988 Dec;25(12):843-6. doi: 10.1136/jmg.25.12.843.
4
先天性角化不良:通过对一组童年期确诊患者的研究了解该疾病的自然史。
Front Pediatr. 2023 Aug 1;11:1182476. doi: 10.3389/fped.2023.1182476. eCollection 2023.
4
Inherited Reticulate Pigmentary Disorders.遗传性网状色素沉着障碍。
Genes (Basel). 2023 Jun 20;14(6):1300. doi: 10.3390/genes14061300.
5
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Am J Surg Pathol. 2023 Aug 1;47(8):869-877. doi: 10.1097/PAS.0000000000002060. Epub 2023 May 29.
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Avascular Peripheral Retina in Infants.婴儿无血管性周边视网膜
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