Huang Hui, Zhang Dongguang, Yang Yu, Yang Li, Chai Yong
Jiangxi Provincial Key Laboratory of Child Development and Genetics, Jiangxi Provincial Children's Hospital (The Affiliated Children's Hospital of Nanchang Medical College), Nanchang, China.
Department of Endocrinology, Metabolism and Genetics, Jiangxi Provincial Children's Hospital (The Affiliated Children's Hospital of Nanchang Medical College), Nanchang, China.
Front Endocrinol (Lausanne). 2025 Jun 27;16:1583190. doi: 10.3389/fendo.2025.1583190. eCollection 2025.
Gabriele-de Vries syndrome (GADEVS, OMIM 617557) is a rare autosomal dominant disorder caused by pathogenic variants in the YY1 gene. This report describes a case of GADEVS with concurrent Hashimoto's thyroiditis (HT) and nanophthalmos, a previously unreported association.
We present a case of a 9-year-5-month-old girl who was admitted to the Pediatric Endocrinology Outpatient Clinic due to an asymptomatic neck lump and multiple malformations.Physical examination revealed mild facial dysmorphism, strabismus, an enlarged thyroid gland, and elongated fingers. Laboratory findings showed: thyroid-stimulating hormone (TSH): 68.98 μIU/mL (reference range: 0.27-4.2 μIU/mL); free thyroxine (FT4): 7.51 pmol/L (reference range: 12-22 pmol/L); anti-thyroid peroxidase antibodies:>600IU/mL (reference range: 0-34 IU/mL). Ultrasonography revealed that the left thyroid lobe measured 38 × 11 × 12 mm, the right lobe 39 × 11 × 13 mm, and the isthmus had a thickness of 3.2 mm. Ocular axial measurements confirmed nanophthalmos, and cognitive assessments indicated mild cognitive impairment. Whole-exome sequencing identified a novel heterozygous YY1 mutation (c.385del), resulting in a frameshift variant (p.D129Ifs*127). Levothyroxine replacement therapy successfully corrected the hypothyroidism. After three years of treatment, the patient exhibited: a height increase of 20.3 cm, and an improvement in height percentile from the 10th to the 25th percentile.
Hypothyroidism has been reported in four previous cases (12%) of GADEVS, but autoimmune thyroiditis has not been documented. This suggests that thyroid dysfunction in GADEVS may be associated with underlying immune dysfunction and warrants further evaluation. In the present case, we identified a mutation in the YY1 gene, which is associated with nanophthalmos and may underlie the ocular abnormalities such as strabismus and hyperopia. Clinically, children with GADEVS should undergo comprehensive assessments of thyroid function, thyroid autoantibodies, and ophthalmologic status to facilitate early diagnosis and treatment.
加布里埃莱 - 德弗里斯综合征(GADEVS,OMIM 617557)是一种由YY1基因的致病变异引起的罕见常染色体显性疾病。本报告描述了一例并发桥本甲状腺炎(HT)和小眼球症的GADEVS病例,这是一种此前未报告过的关联。
我们报告一例9岁5个月大的女孩,因无症状颈部肿块和多种畸形入住儿科内分泌门诊。体格检查发现轻度面部畸形、斜视、甲状腺肿大和手指细长。实验室检查结果显示:促甲状腺激素(TSH):68.98 μIU/mL(参考范围:0.27 - 4.2 μIU/mL);游离甲状腺素(FT4):7.51 pmol/L(参考范围:12 - 22 pmol/L);抗甲状腺过氧化物酶抗体:>600IU/mL(参考范围:0 - 34 IU/mL)。超声检查显示左甲状腺叶大小为38×11×12 mm,右叶为39×11×13 mm,峡部厚度为3.2 mm。眼轴测量证实为小眼球症,认知评估表明存在轻度认知障碍。全外显子测序鉴定出一种新的杂合YY1突变(c.385del),导致移码变异(p.D129Ifs*127)。左甲状腺素替代疗法成功纠正了甲状腺功能减退。经过三年治疗,患者身高增加了20.3 cm,身高百分位从第10百分位提高到第25百分位。
此前报道的4例GADEVS病例(12%)中出现了甲状腺功能减退,但自身免疫性甲状腺炎尚未有记录。这表明GADEVS中的甲状腺功能障碍可能与潜在的免疫功能障碍有关,值得进一步评估。在本病例中,我们鉴定出YY1基因的一个突变,该突变与小眼球症相关,可能是斜视和远视等眼部异常的基础。临床上,GADEVS患儿应接受甲状腺功能、甲状腺自身抗体和眼科状况的综合评估,以促进早期诊断和治疗。