Cargando…
A 18p11.23-p11.31 microduplication in a boy with psychomotor delay, cerebellar vermis hypoplasia, chorioretinal coloboma, deafness and GH deficiency
BACKGROUND: Rearrangements involving the short arm of chromosome 18 have been extensively described. Here we report a microduplication of 320.5–431.5 Kb at 18p11.31-p11.23 in a 10 year-old boy. CASE PRESENTATION: In a 10 year-old boy with moderate psychomotor delay, hypoplasia of the cerebellar verm...
Autores principales: | Giordano, Mara, Muratore, Valentina, Babu, Deepak, Meazza, Cristina, Bozzola, Mauro |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5135744/ https://www.ncbi.nlm.nih.gov/pubmed/27980677 http://dx.doi.org/10.1186/s13039-016-0298-9 |
Ejemplares similares
-
7q11.23 Microduplication Syndrome: Clinical and Neurobehavioral Profiling
por: Dentici, Maria Lisa, et al.
Publicado: (2020) -
Intrauterine phenotype features of fetuses with 7q11.23 microduplication syndrome
por: Wang, Yunan, et al.
Publicado: (2023) -
A novel case of global developmental delay syndrome with microdeletion at 10p14–p15.3 and microduplication at 18p11.31–p11.32
por: Zhang, Danyan, et al.
Publicado: (2019) -
20p11.23-p11.21 deletion in a child with hyperinsulinemic hypoglycemia and GH
deficiency: A case report
por: Sugawara, Daisuke, et al.
Publicado: (2021) -
Confirming and expanding the phenotypes of FZD5 variants: Coloboma, inferior chorioretinal hypoplasia, and high myopia
por: Jiang, Yi, et al.
Publicado: (2021)