H

Hulya Kose1, Merve Deniz Baskaya1, Sara Sebnem Kilic1

  • 1Department of Pediatric Immunology and Rheumatology, Uludag University Faculty of Medicine, Bursa, Turkey.

概括

H综合征是一种由SLC29A3基因突变引起的遗传疾病,呈现出多颜色和听力损失. 这项研究详细介绍了两个病例,扩大已知的临床特征,包括关节炎和骨密度问题.

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