Cargando…
An Interstitial Deletion at 7q33-36.1 in a Patient with Intellectual Disability, Significant Language Delay, and Severe Microcephaly
Interstitial deletions of the distal 7q region are considered a rare entity. In this report, we describe a seven-year-old male with a heterozygous interstitial deletion at 7q33-36.1 with characteristic dysmorphic facial features, intellectual disability, severe microcephaly, and significant language...
Autores principales: | Kale, Trupti, Philip, Melissa |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5178345/ https://www.ncbi.nlm.nih.gov/pubmed/28053794 http://dx.doi.org/10.1155/2016/6046351 |
Ejemplares similares
-
Deletion of 7q33-q35 in a Patient with Intellectual Disability and Dysmorphic Features: Further Characterization of 7q Interstitial Deletion Syndrome
por: Dilzell, Kristen, et al.
Publicado: (2015) -
Two new cases of interstitial 7q35q36.1 deletion including CNTNAP2 and KMT2C
por: Tosca, Lucie, et al.
Publicado: (2021) -
Patient With Delayed Development Resulting From De Novo Duplication of 7q36.1-q36.3 and Deletion of 9p24.3
por: Choi, Asayeon, et al.
Publicado: (2017) -
Deletion at 12q12 increases the risk of developmental delay and intellectual disability
por: Weng, Ying, et al.
Publicado: (2018) -
7q35 Microdeletion and 15q13.3 and Xp22.33 Microduplications in a Patient with Severe Myoclonic Epilepsy, Microcephaly, Dysmorphisms, Severe Psychomotor Delay and Intellectual Disability
por: Paduano, Francesco, et al.
Publicado: (2020)