一名患有斯内登综合征的8岁儿童：罕见病例报告。
An Eight-Year-Old Child With Sneddon Syndrome: A Rare Case Report.
作者信息
Nallur Siddaraju Maheshwari, Samynathan Archana, Kurakula Sowjanya, Kharge Priyadarshini, Nalla Sanjana D
机构信息
Dermatology, Bangalore Medical College and Research Institute, Bangalore, IND.
Dermatology, George Washington University, Virginia, USA.
出版信息
Cureus. 2023 Jun 6;15(6):e40054. doi: 10.7759/cureus.40054. eCollection 2023 Jun.
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.
我们报告了一例罕见的进展缓慢的神经皮肤血管病变，称为斯内登综合征。一名儿童出现全面发育迟缓、先天性网状青斑、单眼视力丧失，以及既往有局灶性神经功能缺损病史。我们的主要目的是让医生了解儿童这种表现的性质。
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