Double Isochromosome X, a Rare Cytogenetic Variant of Turner Syndrome: A Case Report and a Review of the Literature

Turner Syndrome (TS) is a genetic disorder caused by total or partial loss of an X chromosome. The isochromosome X (i(X)) is a known variant of TS, however, double i(X) is a very rare variant, reported very few times in the literature. We report on a rare case of TS with double i(X). This is an 11-y...

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Detalles Bibliográficos
Autores principales: Zerrouki, K., Elidrissi, Errahhali M., Babakhouya, A., Tajir, M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sciendo 2023
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985355/
https://www.ncbi.nlm.nih.gov/pubmed/36880033
http://dx.doi.org/10.2478/bjmg-2022-0011

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9985355/
https://www.ncbi.nlm.nih.gov/pubmed/36880033
http://dx.doi.org/10.2478/bjmg-2022-0011

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