Department of Pediatric Immunology and Rheumatology, Uludag University Faculty of Medicine, Bursa, Turkey.
Australas J Dermatol. 2024 Jun;65(4):337-341. doi: 10.1111/ajd.14235. Epub 2024 Feb 29.
The H syndrome is an autosomal recessive disease characterized by hyperpigmentation, hypertrichosis and sensorineural hearing loss.
A mutation in the coding of the human equilibrative nucleoside transporter 3 (hENT3) within the SLC29A3 gene on chromosome 10q22 leads to the manifestation of this disease. In this report, we present two cases of H syndrome.
The first patient exhibits hyperpigmentation, hypogonadism, Type 1 diabetes mellitus, arthritis and osteoporosis. The second patient experiences hyperpigmentation, hypertrichosis, osteopenia and hypogonadism.
Our objective is to broaden the clinical spectrum of H syndrome, highlighting the involvement of arthritis, hyperinflammation and low bone mineral density in individuals with this disorder.
H 综合征是一种常染色体隐性遗传病,其特征为色素沉着过度、多毛症和感觉神经性耳聋。
编码人类平衡核苷转运蛋白 3(hENT3)的基因突变导致了 10q22 染色体上 SLC29A3 基因的表现,这导致了这种疾病的发生。在本报告中,我们介绍了两例 H 综合征病例。
第一例患者表现为色素沉着过度、性腺功能减退症、1 型糖尿病、关节炎和骨质疏松症。第二例患者表现为色素沉着过度、多毛症、骨质疏松症和性腺功能减退症。
我们的目的是拓宽 H 综合征的临床谱,强调关节炎、高炎症和低骨密度矿物质在患有这种疾病的个体中的参与。