Turner syndrome due to Xp22.33 deletion with preserved gonadal function: case report

Turner syndrome (TS) is a chromosomal condition affecting 1 in 2000 females characterized by partial or complete loss of one of the X chromosomes. We describe an 11-year-old female who was recently diagnosed with TS. Karyotype revealed a deletion of the distal portion of chromosome X. Chromosome sin...

Descripción completa

Detalles Bibliográficos
Autores principales: D’Ambrosio, Fabiola, Chan, Jacqueline T, Aslam, Hunain, Aguirre Castaneda, Roxana, De Simone, Lenika, Shad, Zohra
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570789/
https://www.ncbi.nlm.nih.gov/pubmed/31214355
http://dx.doi.org/10.1093/omcr/omz028

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6570789/
https://www.ncbi.nlm.nih.gov/pubmed/31214355
http://dx.doi.org/10.1093/omcr/omz028

Ejemplares similares