A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature

We present a complex chromosomal anomaly identified using cytogenetic and molecular methods. The child was diagnosed during the neonatal period with a multiple congenital anomalies syndrome characterized by: flattened occipital region; slight turricephaly; tall and broad forehead; hypertelorism; dee...

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Detalles Bibliográficos
Autores principales: Popescu, Roxana, Grămescu, Mihaela, Caba, Lavinia, Pânzaru, Monica-Cristina, Butnariu, Lăcrămioara, Braha, Elena, Popa, Setalia, Rusu, Cristina, Cardos, Georgeta, Zeleniuc, Monica, Martiniuc, Violeta, Gug, Cristina, Păduraru, Luminiţa, Stamatin, Maria, Diaconu, Carmen C., Gorduza, Eusebiu Vlad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701147/
https://www.ncbi.nlm.nih.gov/pubmed/34946906
http://dx.doi.org/10.3390/genes12121957

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701147/
https://www.ncbi.nlm.nih.gov/pubmed/34946906
http://dx.doi.org/10.3390/genes12121957

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