SHOX Duplication and Tall Stature in a Patient with Xq Deletion and Vascular Disease

JÉSICA RAMÍREZ; ANALÍA VARGAS; NICOLÁS RENNA; RODRIGUEZ FA; ADRIANA CALDERÓN; MARÍA INÉS ECHEVERRÍA; MIATELLO, ROBERTO MIGUEL

Case Reports in Genetics

Hindawi

Lugar: London; Año: 2019 vol. 2019 p. 1 - 7

2090-6544

The anomalies of X chromosome are classified as numerical or structural. Concomitant structural anomalies in this chromosomethat associate partial loss of its long arm with duplications in its short arm are uncommon. Only a few cases have been publishedand in most of them the reported patients present ovarian dysfunction, tall stature, and overdosage of the SHOX gene with locusXp22.33. Considering these reports, we evaluated the case of a woman with a deletion in the long arm of the X chromosome, premature ovarian failure, tall stature, and multiple arterial vascular disease.With the aimto find a relationship between karyotype and phenotype, we explored associated anomalies in Xp and certified the overdosage of the SHOX gene in this case byMLPA. Also,taking into account the fact that the gene locus of the angiotensin-converting enzyme type 2 (ACE2) is located in Xp, our goal was to investigate the influence of this gene in the development of cardiovascular disease. The detection of the gene product of ACE2 by ELISA was undetectable.We have proposed that cytogenetic anomalies in X chromosome could contribute to decrease this protein synthesis in this gender.