与特发性婴儿皮质增生症（卡菲病）相关的威斯科特-奥尔德里奇综合征。 - Suppr

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超能文献

Wiskott-Aldrich syndrome associated with idiopathic infantile cortical hyperostosis (Caffey's disease).

作者信息

McEnery G, Nash F W

出版信息

Arch Dis Child. 1973 Oct;48(10):818-21. doi: 10.1136/adc.48.10.818.

DOI:10.1136/adc.48.10.818

PMID:4584223

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1648512/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/23b8/1648512/814eea7327f6/archdisch00860-0079-a.jpg

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Wiskott-Aldrich syndrome associated with idiopathic infantile cortical hyperostosis (Caffey's disease).与特发性婴儿皮质增生症（卡菲病）相关的威斯科特-奥尔德里奇综合征。

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The Wiskott-Aldrich syndrome.维斯科特-奥尔德里奇综合征

Clin Rev Allergy Immunol. 2001 Feb;20(1):61-86. doi: 10.1385/CRIAI:20:1:61.

Caffey disease responding to high-dose immunoglobulin.卡菲病对大剂量免疫球蛋白治疗有反应。

Eur J Pediatr. 1988 May;147(4):443-4. doi: 10.1007/BF00496434.

Infantile cortical hyperostosis associated with the Wiskott-Aldrich syndrome.与威斯科特-奥尔德里奇综合征相关的婴儿皮质增生症。

Eur J Pediatr. 1988 Jun;147(5):518-9. doi: 10.1007/BF00441979.

本文引用的文献

Aldrich's syndrome. Report of a case with subperiosteal hemorrhage.

J Pediatr. 1960 Jul;57:86-8. doi: 10.1016/s0022-3476(60)80215-6.

Familial infantile cortical hyperostosis.家族性婴儿皮质增生症

J Pediatr. 1961 Oct;59:543-8. doi: 10.1016/s0022-3476(61)80238-2.

Pedigree demonstrating a sex-linked recessive condition characterized by draining ears, eczematoid dermatitis and bloody diarrhea.系谱显示一种X连锁隐性疾病，其特征为耳漏、湿疹样皮炎和血性腹泻。

Pediatrics. 1954 Feb;13(2):133-9.

Serum levels of immune globulins in health and disease: a survey.健康与疾病状态下血清免疫球蛋白水平：一项调查

Pediatrics. 1966 May;37(5):715-27.

Raised immunoglobulin levels and thrombocytosis in infantile cortical hyperostosis.

Arch Dis Child. 1972 Dec;47(256):982-3. doi: 10.1136/adc.47.256.982.

Infantile cortical hyperostosis associated with thrombocythaemia.婴儿皮质增生症伴血小板增多症

Lancet. 1969 Aug 30;2(7618):464-5. doi: 10.1016/s0140-6736(69)90168-8.

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