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Recessive metaphyseal dysplasia without hypotrichosis. A syndrome clinically distinct from McKusick cartilage-hair hypoplasia.

作者信息

Verloes A, Pierard G E, Le Merrer M, Maroteaux P

机构信息

Centre for Human Genetics, Liège University, Belgium.

出版信息

J Med Genet. 1990 Nov;27(11):693-6. doi: 10.1136/jmg.27.11.693.

DOI:10.1136/jmg.27.11.693
PMID:2277385
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1017260/
Abstract

Among children with recessive metaphyseal dysplasia involving the knees and extremities, two types can be distinguished. In true cartilage-hair hypoplasia, as described by McKusick, many patients show clinical hair involvement and variable immunodeficiency. We present a series of six patients with the same radiological changes, but without apparent hypotrichosis. We suggest that they should be considered as having a variant form of cartilage-hair hypoplasia, with a clinically distinct phenotype, which could be as common as 'true' cartilage-hair hypoplasia among non-Amish populations. Microscopic examination of the hair may show reduction in the diameter of the hair shaft. This form of metaphyseal dysplasia may result from allelic heterogeneity.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/4d4998ff1f2b/jmedgene00049-0032-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/469a349d7050/jmedgene00049-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/e9b423ecc855/jmedgene00049-0030-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/5006f2ec7fe8/jmedgene00049-0030-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/4edf10eb0a70/jmedgene00049-0030-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/b52c4f9f3170/jmedgene00049-0031-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/e65025d832bd/jmedgene00049-0031-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/72ed23a615bc/jmedgene00049-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/4d4998ff1f2b/jmedgene00049-0032-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/469a349d7050/jmedgene00049-0029-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/e9b423ecc855/jmedgene00049-0030-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/5006f2ec7fe8/jmedgene00049-0030-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/4edf10eb0a70/jmedgene00049-0030-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/b52c4f9f3170/jmedgene00049-0031-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/e65025d832bd/jmedgene00049-0031-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/72ed23a615bc/jmedgene00049-0032-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/45a4/1017260/4d4998ff1f2b/jmedgene00049-0032-b.jpg

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本文引用的文献

1
DWARFISM IN THE AMISH. II. CARTILAGE-HAIR HYPOPLASIA.阿米什人中的侏儒症。II. 软骨毛发发育不全。
Bull Johns Hopkins Hosp. 1965 May;116:285-326.
核糖体生物合成在骨骼发育及骨骼疾病发病机制中的作用
Biochim Biophys Acta. 2014 Jun;1842(6):769-78. doi: 10.1016/j.bbadis.2013.11.010. Epub 2013 Nov 16.
4
When ribosomes go bad: diseases of ribosome biogenesis.当核糖体出现故障时:核糖体生物合成疾病
Mol Biosyst. 2010 Mar;6(3):481-93. doi: 10.1039/b919670f. Epub 2010 Jan 11.
5
Identification of novel RMRP mutations and specific founder haplotypes in Japanese patients with cartilage-hair hypoplasia.日本软骨毛发发育不全患者中新型RMRP突变和特定奠基者单倍型的鉴定。
J Hum Genet. 2006;51(8):706-710. doi: 10.1007/s10038-006-0015-3. Epub 2006 Jul 11.
6
Genetic changes in the RNA components of RNase MRP and RNase P in Schmid metaphyseal chondrodysplasia.施密德干骺端软骨发育不良中核糖核酸酶MRP和核糖核酸酶P的RNA成分的基因变化。
J Med Genet. 2003 Oct;40(10):741-6. doi: 10.1136/jmg.40.10.741.
7
Cartilage-hair hypoplasia--clinical manifestations in 108 Finnish patients.软骨毛发发育不全——108例芬兰患者的临床表现
Eur J Pediatr. 1993 Mar;152(3):211-7. doi: 10.1007/BF01956147.
8
Cartilage hair hypoplasia in infancy: a misleading chondrodysplasia.婴儿期软骨毛发发育不全:一种易误导的软骨发育异常。
Eur J Pediatr. 1991 Oct;150(12):847-51. doi: 10.1007/BF01955006.