Cargando…
Chromosome 3q29 deletion with gastrointestinal malformation: a case report
INTRODUCTION: Most chromosome 3 deletions are associated with neuro-developmental and eye abnormalities. Here, we report a rare and unusual multiple congenital abnormality, including ano-rectal malformation, in conjunction with chromosome 3q29 segment deletion, which has not previously been reported...
Autor principal: | Masarweh, Ma'in |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3141721/ https://www.ncbi.nlm.nih.gov/pubmed/21729261 http://dx.doi.org/10.1186/1752-1947-5-285 |
Ejemplares similares
-
A novel proximal 3q29 chromosome microdeletion in a Chinese patient with Chiari malformation type II and Sprengel’s deformity
por: Guo, Shuai, et al.
Publicado: (2018) -
Comprehensive phenotyping of neuropsychiatric traits in a multiplex 3q29 deletion family: a case report
por: Murphy, Melissa M., et al.
Publicado: (2020) -
A Novel 3q29 Deletion in Association With Developmental Delay and Heart Malformation—Case Report With Literature Review
por: Chirita Emandi, Adela, et al.
Publicado: (2019) -
Chromosome 11q13 deletion syndrome
por: Kim, Yu-Seon, et al.
Publicado: (2016) -
Novel Vascular Malformation in an Affected Newborn with Deletion Del(4)(q31.3)
por: de León Ojeda, Norma Elena, et al.
Publicado: (2012)