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Swiss agammaglobulinemia with hypoglycemia, osseous changes and eosinophilia.

作者信息

Duic A, Crozier D N, Lynch M J, McClure P D

出版信息

Can Med Assoc J. 1970 Jul 4;103(1):64-8 passim.

PMID:5424299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1930334/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/67e50bf6904b/canmedaj01597-0069-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/70f35ab46ee9/canmedaj01597-0066-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/0e442ba17442/canmedaj01597-0067-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/88ee6cebc17b/canmedaj01597-0067-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/9d6d3db88896/canmedaj01597-0068-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/232af360023b/canmedaj01597-0068-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/b111ecc0561e/canmedaj01597-0068-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/4066cab06a20/canmedaj01597-0069-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/67e50bf6904b/canmedaj01597-0069-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/70f35ab46ee9/canmedaj01597-0066-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/0e442ba17442/canmedaj01597-0067-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/88ee6cebc17b/canmedaj01597-0067-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/9d6d3db88896/canmedaj01597-0068-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/232af360023b/canmedaj01597-0068-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/b111ecc0561e/canmedaj01597-0068-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/4066cab06a20/canmedaj01597-0069-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9a9/1930334/67e50bf6904b/canmedaj01597-0069-b.jpg

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Swiss agammaglobulinemia with hypoglycemia, osseous changes and eosinophilia.伴有低血糖、骨质改变和嗜酸性粒细胞增多的瑞士无丙种球蛋白血症。
Can Med Assoc J. 1970 Jul 4;103(1):64-8 passim.
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Heterogeneity of phenotypic expression in a family with Swiss-type agammaglobulinemia: observations on the acquisition of agammaglobulinemia.
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引用本文的文献

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Hypothermia, hypoglycemia, and hypothyrosis associated with poult enteritis and mortality syndrome.与雏禽肠炎和死亡综合征相关的体温过低、低血糖和甲状腺功能减退。
Poult Sci. 1998 Aug;77(8):1103-9. doi: 10.1093/ps/77.8.1103.
2
Liver necrosis, adenovirus type 2 and thymic dysplasia.肝坏死、2型腺病毒与胸腺发育不良。
Virchows Arch A Pathol Pathol Anat. 1973 Aug 9;360(2):155-71. doi: 10.1007/BF00543226.
3
Effect of eosinophil-degranulating estrogens on spleen eosinophils and white pulp/red pulp ratio.嗜酸性粒细胞脱颗粒雌激素对脾脏嗜酸性粒细胞及白髓/红髓比例的影响。

本文引用的文献

1
[Essential lymphocytophthisis; new clinical aspect of infant pathology].[原发性淋巴细胞消耗症;婴儿病理学的新临床方面]
Ann Paediatr. 1950 Jul-Aug;175(1-2):1-32.
2
Agammaglobulinemia.无丙种球蛋白血症
Pediatrics. 1952 Jun;9(6):722-8.
3
Alymphocytosis, agammaglobulinaemia, homografts, and delayed hypersen sitivity: study of a case.无淋巴细胞血症、无丙种球蛋白血症、同种移植及迟发型超敏反应:1例研究
Agents Actions. 1990 Nov;31(3-4):249-56. doi: 10.1007/BF01997616.
Lancet. 1962 Aug 25;2(7252):380-1. doi: 10.1016/s0140-6736(62)90232-5.
4
[HEREDITARY THYMIC HYPOPLASIA: ITS PLACE AND RESPONSIBILITY IN A CASE OF LYMPHOCYTIC, NORMOPLASMOCYTIC AND NORMOGLOBULINEMIC APLASIA IN AN INFANT].[遗传性胸腺发育不全:在一名婴儿淋巴细胞、正常浆细胞和正常球蛋白血症性再生障碍性贫血病例中的地位及作用]
Arch Fr Pediatr. 1964 Oct;21:897-920.
5
THE THYMUS AND OTHER LYMPHOID TISSUES IN CONGENITAL AGAMMAGLOBULINEMIA. I. THYMIC ALYMPHOPLASIA AND LYMPHOCYTIC HYPOPLASIA AND THEIR RELATION TO INFECTION.先天性无丙种球蛋白血症中的胸腺及其他淋巴组织。I.胸腺淋巴细胞生成障碍和淋巴细胞发育不全及其与感染的关系。
Pediatrics. 1963 Oct;32:517-30.
6
Reticular dysgenesia.网状细胞发育不全
Lancet. 1959 Dec 19;2(7112):1123-5. doi: 10.1016/s0140-6736(59)90105-9.
7
[Agammaglobulinemia & alymphocytosis with atrophy of lymphatic tissue].[无丙种球蛋白血症及淋巴细胞减少伴淋巴组织萎缩]
Helv Paediatr Acta. 1958 Dec;13(6):551-85.
8
Phagocytosis of mast cell granule by the eosinophilic leukocyte in the rat.大鼠嗜酸性白细胞对肥大细胞颗粒的吞噬作用。
Am J Pathol. 1959 Jan-Feb;35(1):103-11.
9
[Familial lymphopenia with agammaglobulinemia & severe moniliasis: the essential lymphocytophthisis as a special form of early childhood agammaglobulinemia].[伴有无丙种球蛋白血症和严重念珠菌病的家族性淋巴细胞减少症:作为幼儿期无丙种球蛋白血症一种特殊形式的原发性淋巴细胞消耗症]
Helv Paediatr Acta. 1958 Oct;13(4):313-38.
10
Thymic dysplasia ("Swiss agammaglobulinemia"). II. Morphologic and functional observations.
J Pediatr. 1967 May;70(5):737-44. doi: 10.1016/s0022-3476(67)80324-x.