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The nature of agenesis and deficiency of parts; the influence of intrinsic factors in disease when development of the body is abnormal, as illustrated by agenesis of the digits, facial hemiatrophy, and cerebral agyria and microgyria.

作者信息

INGLIS K

出版信息

Am J Pathol. 1952 May-Jun;28(3):449-75.

PMID:14923835
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1937351/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/2f1658863933/amjpathol00488-0149-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/2f9000ad136d/amjpathol00488-0145-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/088c1edb8542/amjpathol00488-0145-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/766c3f086637/amjpathol00488-0145-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/5a9c8d515eeb/amjpathol00488-0145-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/aa1f392f8a3b/amjpathol00488-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/bfc31e94f6bc/amjpathol00488-0147-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/79679d709866/amjpathol00488-0147-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/ecad8d3d554f/amjpathol00488-0147-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/2f1658863933/amjpathol00488-0149-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/2f9000ad136d/amjpathol00488-0145-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/088c1edb8542/amjpathol00488-0145-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/766c3f086637/amjpathol00488-0145-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/5a9c8d515eeb/amjpathol00488-0145-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/aa1f392f8a3b/amjpathol00488-0147-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/bfc31e94f6bc/amjpathol00488-0147-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/79679d709866/amjpathol00488-0147-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/ecad8d3d554f/amjpathol00488-0147-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fee6/1937351/2f1658863933/amjpathol00488-0149-a.jpg

相似文献

1
The nature of agenesis and deficiency of parts; the influence of intrinsic factors in disease when development of the body is abnormal, as illustrated by agenesis of the digits, facial hemiatrophy, and cerebral agyria and microgyria.器官发育不全及部分组织缺失的本质；当身体发育异常时内在因素在疾病中的影响，如手指发育不全、面部偏侧萎缩以及大脑回发育不全和小脑回畸形所例证。
Am J Pathol. 1952 May-Jun;28(3):449-75.
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[Case of maxillary agenesis with facial hemiatrophy during infantile polyarthritis].[婴儿型多关节炎期间上颌骨发育不全伴面部半侧萎缩病例]
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Clinical features of 21 patients with lissencephaly type I (agyria-pachygyria).21例Ⅰ型无脑回畸形（无脑回-巨脑回畸形）患者的临床特征
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Intracranial findings in progressive facial hemiatrophy.
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[Facial hemiatrophy with scleroderma and organic brain disorders].[伴有硬皮病和器质性脑障碍的面部半侧萎缩]
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[ASYMMETRY OF THE FACE].[面部不对称]
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引用本文的文献

1
Bibliography of human genetics.人类遗传学文献目录。
Am J Hum Genet. 1953 Jun;5(2):186-91.

本文引用的文献

1
Otosclerosis associated with Fragilitas Ossium and Blue Sclerotics, with a Clinical Report of Three Cases.
Proc R Soc Med. 1919;12(Otol Sect):126-33. doi: 10.1177/003591571901201121.
2
Neurilemmoblastosis; the influence of intrinsic factors in disease when development of the body is abnormal.神经母细胞瘤；当身体发育异常时，内在因素在疾病中的影响。
Am J Pathol. 1950 Jul;26(4):521-49.
3
Renal dysplasia in a family with multiple hereditary abnormalities including iliac horns.一个患有包括髂角在内的多种遗传性异常的家族中的肾发育异常。
Lancet. 1950 Apr 29;1(6609):803-8. doi: 10.1016/s0140-6736(50)90636-2.
4
Localized panatrophy.局限性全身萎缩
Proc R Soc Med. 1950 Mar;43(3):179-80. doi: 10.1177/003591575004300312.
5
Hereditary ataxia with optic atrophy of the retrobulbar neuritis type, and latent pallido-luysian degeneration.球后视神经炎型遗传性共济失调伴视神经萎缩，以及隐匿性苍白球-路易体变性。
Brain. 1949 Sep;72(3):340-63, illust. doi: 10.1093/brain/72.3.340.