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.

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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
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article

Short Stature in Klinefelter Syndrome From Aggrecan Mutation

Sunitha R. Sura, Antoinette Farrell
JCEM Case Reports
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
article

Short Stature in Klinefelter Syndrome From Aggrecan Mutation

Sunitha R. Sura, Antoinette Farrell
article en

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 <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.

JCEM Case ReportsVol. 2(10)
University of Connecticut (US), University of Hartford (US), Connecticut Children's Medical Center (US)
Openalex Percentile: Top 81%
Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
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