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SLC29A3 谱紊乱四种特征合并于儿童:病例报告。

Combination of four features of SLC29A3 spectrum disorder in a child: A case report.

机构信息

Pediatric Rheumatology Society of Iran, Tehran, Iran.

Department of Pediatrics, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Pediatr Dermatol. 2024 Sep-Oct;41(5):888-892. doi: 10.1111/pde.15619. Epub 2024 Apr 30.

Abstract

SLC29A3 spectrum disorder, also known as histiocytosis-lymphadenopathy plus syndrome (HLPS), presents a wide variety of multi-systemic manifestations that can be mistaken for other conditions. Herein, we report a 9-year-old girl who presented with a complex clinical presentation since birth, including chronic generalized lymphadenopathy in association with hepatosplenomegaly, short stature, flexion contractures, hearing loss, hyperpigmentation, and heart anomalies. She was ultimately diagnosed with the SLC29A3 spectrum disorder.

摘要

SLC29A3 谱障碍,也称为组织细胞-淋巴结病综合征(HLPS),表现出广泛的多系统表现,可能被误诊为其他疾病。在此,我们报告了一例 9 岁女孩,自出生以来表现出复杂的临床表现,包括慢性全身性淋巴结病伴肝脾肿大、身材矮小、屈曲挛缩、听力损失、色素沉着过度和心脏异常。她最终被诊断为 SLC29A3 谱障碍。

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