Short Stature in Klinefelter Syndrome From Aggrecan Mutation
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 <i>ACAN</i> 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.
Authors
- Sunitha R. Sura (ORCID: https://orcid.org/0000-0001-5364-9151)
- Antoinette Farrell (ORCID: https://orcid.org/0009-0002-9180-9691)
Institutions
- University of Connecticut (US)
- University of Hartford (US)
- Connecticut Children's Medical Center (US)
Publication Details
- Journal
- JCEM Case Reports
- Published
- 2024-09-18
- DOI
- https://doi.org/10.1210/jcemcr/luae170
- Primary Topic
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00