De Novo Trisomy 1q10q23.3 Mosaicism Causes Microcephaly, Severe Developmental Delay, and Facial Dysmorphic Features but No Cardiac Anomalies

Proximal duplications of chromosome 1q are rare chromosomal abnormalities. Most patients with this condition present with neurological, urogenital, and congenital heart disease and short life expectancy. Mosaicism for trisomy 1q10q23.3 has only been reported once in the literature. Here we discuss a...

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Detalles Bibliográficos
Autores principales: Lo-A-Njoe, Shirley, van der Veken, Lars T., Vermont, Clementien, Rafael-Croes, Louise, Keizer, Vincent, Hochstenbach, Ron, Knoers, Nine, van Haelst, Mieke M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2016
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752968/
https://www.ncbi.nlm.nih.gov/pubmed/26942023
http://dx.doi.org/10.1155/2016/2861653

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4752968/
https://www.ncbi.nlm.nih.gov/pubmed/26942023
http://dx.doi.org/10.1155/2016/2861653

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