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先天性钙化性软骨发育不良(康拉迪 - 许纳曼综合征)的超微结构特征

Ultrastructural aspects of chondrodystrophia calcificans congenita (syndrome of Conradi-Hünermann).

作者信息

Bosman C, Bonucci E, Gugliantini P, Saguì L

出版信息

Virchows Arch A Pathol Anat Histol. 1977 Feb 18;373(1):23-35. doi: 10.1007/BF00432466.

DOI:10.1007/BF00432466
PMID:139022
Abstract

An ultrastructural study of chondrodystrophia calcificans congenita is reported. Foci of initial calcification of cartilage are characterized by coexistence of three different types of crystals, probably due to abnormal proteoglycan composition of cartilage matrix. The calcification process in chondrodystrophia calcificans congenita is apparently not related to 'matrix vesicles' as it is in normal cartilage.

摘要

本文报道了先天性钙化性软骨发育不良的超微结构研究。软骨初始钙化灶的特征是三种不同类型晶体共存,这可能是由于软骨基质蛋白聚糖组成异常所致。先天性钙化性软骨发育不良中的钙化过程显然与正常软骨中的“基质小泡”无关。

相似文献

1
Ultrastructural aspects of chondrodystrophia calcificans congenita (syndrome of Conradi-Hünermann).先天性钙化性软骨发育不良(康拉迪 - 许纳曼综合征)的超微结构特征
Virchows Arch A Pathol Anat Histol. 1977 Feb 18;373(1):23-35. doi: 10.1007/BF00432466.
2
Ichthyosis and keratotic follicular plugs containing dystrophic calcification in newborns: distinctive histopathologic features of x-linked dominant chondrodysplasia punctata (Conradi-Hünermann-Happle syndrome).新生儿鱼鳞病及含有营养不良性钙化的角化性毛囊栓:X连锁显性点状软骨发育不良(康拉迪-于厄尔曼-哈普尔综合征)的独特组织病理学特征
Am J Dermatopathol. 2004 Feb;26(1):53-8. doi: 10.1097/00000372-200402000-00007.
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[Histological ocular findings in chondrodystrophia calcificans congenita (Conradi-Hünermann syndrome)].[先天性钙化性软骨发育不良(康拉迪-许纳曼综合征)的眼部组织学表现]
Ber Zusammenkunft Dtsch Ophthalmol Ges. 1968;68:444-51.
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[Cataract in chondrodystrophia calcificans congenita (Conradi-Hünermann syndrome)].[先天性钙化性软骨发育不良(康拉迪 - 许纳曼综合征)中的白内障]
Klin Monbl Augenheilkd. 1969 Apr;154(4):536-45.
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[AN ADDITIONAL CASE OF CHONDRODYSTROPHIA CALCIFICANS CONGENITA (CONRADI-HUENERMANN SYNDROME)].[先天性钙化性软骨发育不良(康拉迪-许内曼综合征)的另一病例]
Arch Kinderheilkd. 1964 Aug;171:79-83.
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[Chondrodystrophia calcificans congenita (Conradi-Hünermann syndrome). A case report (author's transl)].[先天性钙化性软骨营养障碍(康拉迪-许纳曼综合征)。病例报告(作者译)]
Acta Chir Orthop Traumatol Cech. 1978 Feb;45(1):6-9.
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Chondrodystrophia calcificans congenita (dysplasia epiphysalis punctata). Recognition of the clinical picture.先天性钙化性软骨营养障碍(点状骨骺发育异常)。临床表现的识别。
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Chondrodystrophia calcificans congenita (the conradi-hunermann syndrome). Report of a case recognized antenatally.先天性钙化性软骨营养障碍(康拉迪-于纳曼综合征)。1例产前确诊病例报告。
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[CONTRIBUTION TO THE CLINICAL PICTURE OF CHONDRODYSTROPHIA CALCIFICANS CONGENITA (CONRADI-HUENERMANN)].[对先天性钙化性软骨发育不良(康拉迪-许纳曼病)临床症状的贡献]
Z Kinderheilkd. 1964 Nov 17;91:282-96.
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[CHONDRODYSTROPHIA CALCIFICANS CONGENITA].[先天性钙化性软骨发育不良]
Cesk Rentgenol. 1964 May;18:208-11.

本文引用的文献

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[Congenital disease of stippled epiphyses or fetal chondrodystrophic epiphysial calcinosis].
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Electron microscopic studies of induced cartilage development and calcification.诱导性软骨发育与钙化的电子显微镜研究。
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Heterogeneity of Chondrodysplasia punctata.点状软骨发育不良的异质性。
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Fine structure and histochemistry of "calcifying globules" in epiphyseal cartilage.骨骺软骨中“钙化小球”的精细结构与组织化学
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Chondrodystrophia calcificans congenita (dysplasia epiphysalis punctata). Recognition of the clinical picture.先天性钙化性软骨营养障碍(点状骨骺发育异常)。临床表现的识别。
Am J Dis Child. 1970 Feb;119(2):122-7. doi: 10.1001/archpedi.1970.02100050124006.
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[Chondrodysplasia punctata (Chondrodystrophia calcificans) II. The rhizomelic type].点状软骨发育不良(钙化性软骨营养障碍)II型。肢根型
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The locus of initial calcification in cartilage and bone.
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Theories of mineralization of bone.
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