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[Hypergammaglobulinemia D and familial urticaria in children].

作者信息

Bader-Meunier B, Venencie P Y, Vieillefond A, Le Touze P, Dommergues J P

机构信息

Service de Pédiatrie générale, Hôpital Bicêtre, Le Kremlin Bicêtre.

出版信息

Ann Dermatol Venereol. 1996;123(6-7):398-400.

PMID:8959065
Abstract

OBJECTIVE

Recall the main elements suggesting the diagnosis of hyperimmunoglobulinemia D based on a family case of chronic urticaria.

CASE REPORT

A boy and his mother presented the same signs of urticaria, fever and joint pain. Laboratory results showed an inflammatory syndrome in both. In the child, the first manifestations occurred during the age of one year. Hyperimmunoglobulinemia D was confirmed by persistently high serum levels.

CONCLUSION

The diagnosis of hyperimmunoglobuliemia D can be entertained in a child in a family with chronic urticaria. Fever, joint pain, digestive disorders and enlarged lymph nodes are suggestive and the diagnosis is confirmed by a clear elevation of serum IgD.

摘要

相似文献

1
[Hypergammaglobulinemia D and familial urticaria in children].
Ann Dermatol Venereol. 1996;123(6-7):398-400.
2
[Hyperimmunoglobulinemia D or periodic fever syndrome. Cutaneous manifestations in 3 cases].
Ann Dermatol Venereol. 1996;123(5):314-21.
3
Henoch-Schönlein purpura in a child with hyperimmunoglobulinemia D and periodic fever syndrome.一名患有高免疫球蛋白D血症和周期性发热综合征的儿童的过敏性紫癜。
Pediatr Dermatol. 2005 Mar-Apr;22(2):138-41. doi: 10.1111/j.1525-1470.2005.22210.x.
4
[Hypergammaglobulinemia D syndrome].
An Med Interna. 2000 Apr;17(4):213-6.
5
First report of macrophage activation syndrome in hyperimmunoglobulinemia D with periodic fever syndrome.高免疫球蛋白D血症伴周期性发热综合征中巨噬细胞活化综合征的首例报告。
Arthritis Rheum. 2007 Feb;56(2):658-61. doi: 10.1002/art.22409.
6
Overt and occult rheumatic diseases: the child with chronic fever.显性和隐匿性风湿性疾病:长期发热的儿童
Best Pract Res Clin Rheumatol. 2002 Jul;16(3):443-69.
7
Pseudodominant inheritance of the hyperimmunoglobulinemia D with periodic fever syndrome in a mother and her two monozygotic twins.一位母亲及其两名同卵双胞胎中高免疫球蛋白D伴周期性发热综合征的假显性遗传。
Arthritis Rheum. 2005 Nov;52(11):3606-10. doi: 10.1002/art.21381.
8
[The hyperimmunoglobulinemia D syndrome].[高免疫球蛋白D综合征]
Cas Lek Cesk. 1991 Mar 8;130(10):305.
9
Cold urticaria associated with C4 deficiency and elevated IgM.与C4缺乏和IgM升高相关的寒冷性荨麻疹
Ann Allergy. 1986 Apr;56(4):313-6.
10
[Hyperimmunoglobulin D syndrome].[高免疫球蛋白D综合征]
Presse Med. 1995 Sep 16;24(26):1211-3.

引用本文的文献

1
New mutations of CIAS1 that are responsible for Muckle-Wells syndrome and familial cold urticaria: a novel mutation underlies both syndromes.导致穆克-韦尔斯综合征和家族性冷荨麻疹的CIAS1新突变:一种新突变是这两种综合征的基础。
Am J Hum Genet. 2002 Jun;70(6):1498-506. doi: 10.1086/340786. Epub 2002 Apr 25.