An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report

被引：0

作者：

Siddaraju, Maheshwari Nallur ^{[1
]}

Samynathan, Archana ^{[1
,2
]}

Kurakula, Sowjanya ^{[3
,4
,5
,6
]}

Kharge, Priyadarshini ^{[1
]}

Nalla, Sanjana D. ^{[7
]}

机构：

[1] Bangalore Med Coll & Res Inst, Dermatol, Bangalore, India

[2] George Washington Univ, Dermatol, Ashburn, VA USA

[3] Mamta Inst Med Sci, Obstet & Gynecol, Khammam, India

[4] Sekgoma Mem Hosp, Obstet & Gynecol, Serowe, Botswana

[5] Nyangabgwe Referral Hosp, Obstet & Gynecol, Francistown, Botswana

[6] Gandhi Med Coll, Obstet & Gynecol, Secunderabad, India

[7] Lake Erie Coll Osteopath Med, Sch Med, Erie, PA USA

来源：

CUREUS JOURNAL OF MEDICAL SCIENCE | 2023年 / 15卷 / 06期

关键词：

Categories; Dermatology; Family; General Practice; Pediatrics livedo racemosa; case report; systemic vasculitis; pediatric stroke; cerebrovascular accident; livedo reticularis;

D O I：

10.7759/cureus.40054

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

We present a rare case of slow-progressing neurocutaneous vasculopathy described as Sneddon syndrome. A child presented with global developmental delay, congenital livedo racemosa, unilateral vision loss, and a past history of focal neurological deficit. Our main objective is to make physicians aware of this nature of presentation in children.

引用

页数：5