Cargando…
Cervical Spine Malformations Associated With a 5q34-5q35.2 Micro-interstitial Deletion: A Case Report
We report a female proband carrying a de novo 5q34-q35.2 deletion breakpoint, and review the unique skeletal phenotype and possible genotype related to this mutation. The patient presented with a persistent head tilt and limited head rotation. Non-contrast-enhanced three-dimensional computed tomogra...
Autores principales: | Lee, Heewon, Kim, Joon Sung, Lim, Seong Hoon, Sul, Bomi, Hong, Bo Young |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Korean Academy of Rehabilitation Medicine
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6325309/ https://www.ncbi.nlm.nih.gov/pubmed/30613082 http://dx.doi.org/10.5535/arm.2018.42.6.884 |
Ejemplares similares
-
Prenatal diagnosis of a 4.5-Mb deletion at chromosome 4q35.1q35.2: Case report and literature review
por: Xiao, Gefei, et al.
Publicado: (2021) -
Report of trisomy 2q34-qter and monosomy 4q35.2-qter in a child with mild dysmorphic syndrome and karyotype 46,XY,der(4)t(2;4)(q34;q35.2)pat
por: Meza-Espinoza, Juan Pablo, et al.
Publicado: (2020) -
Cytogenomic characterization of 1q43q44 deletion associated with 4q32.1q35.2 duplication and phenotype correlation
por: Mohamed, A. M., et al.
Publicado: (2018) -
Unexplained Pancytopenia in a Patient with 5q35.2-q35.3 Microduplication Encompassing NSD1: A Case Report
por: Park, Sungwoo, et al.
Publicado: (2018) -
Evolutionary genomic remodelling of the human 4q subtelomere (4q35.2)
por: Bodega, Beatrice, et al.
Publicado: (2007)