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由聚集蛋白聚糖突变导致的克兰费尔特综合征中的身材矮小

Short Stature in Klinefelter Syndrome From Aggrecan Mutation.

作者信息

Farrell Antoinette, Sura Sunitha R

机构信息

Department of Pediatrics, University of Connecticut School of Medicine, Hartford, CT 06106, USA.

Division of Pediatric Endocrinology & Diabetes, Connecticut Children's, Farmington, CT 06032, USA.

出版信息

JCEM Case Rep. 2024 Oct 3;2(10):luae170. doi: 10.1210/jcemcr/luae170. eCollection 2024 Oct.

Abstract

Despite tall stature being a characteristic feature of Klinefelter syndrome, occasional cases of short stature have been reported. These cases are often attributed to GH deficiency. This case report details a unique case of a 16-year-old male with Klinefelter syndrome exhibiting proportionate short stature resulting from a heterozygous, likely pathogenic, variant in the gene c.7141G > A (p.Asp2381Asn). This specific variant, previously identified once in a family with a recessive inheritance pattern is reported here for the first time in an individual with Klinefelter syndrome. This report emphasizes the importance of a thorough evaluation and consideration of genetic testing for an underlying diagnosis in short-statured individuals with Klinefelter syndrome. Timely detection would enable appropriate therapeutic interventions.

摘要

尽管身材高大是克兰费尔特综合征的一个特征性表现,但偶尔也有身材矮小的病例报道。这些病例通常归因于生长激素缺乏。本病例报告详细介绍了一名16岁克兰费尔特综合征男性的独特病例,该患者因基因c.7141G > A(p.Asp2381Asn)中的杂合、可能致病的变异而出现匀称性身材矮小。这种特定变异此前在一个具有隐性遗传模式的家族中被发现过一次,本文首次报道其出现在一名克兰费尔特综合征患者中。本报告强调了对克兰费尔特综合征身材矮小个体进行全面评估并考虑进行基因检测以明确潜在诊断的重要性。及时检测将有助于采取适当的治疗干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dc3/11447372/d29b455d06f9/luae170f1.jpg

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