Terminal 10q26.12 deletion is associated with neonatal asymmetric crying facies syndrome: a case report and literature review

BACKGROUND: The terminal 10q26 deletion syndrome is a clinically heterogeneous disorder without identified genotype–phenotype correlations. We reported a case of congenital asymmetric crying facies (ACF) syndrome with 10q26.12qter deletion and discussed their genotype–phenotype correlations and the...

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Detalles Bibliográficos
Autores principales: Li, Qinghong, Sun, Chunmei, Guo, Jinzhen, Zhai, Wen, Zhang, Liping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278754/
https://www.ncbi.nlm.nih.gov/pubmed/34256807
http://dx.doi.org/10.1186/s13039-021-00554-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278754/
https://www.ncbi.nlm.nih.gov/pubmed/34256807
http://dx.doi.org/10.1186/s13039-021-00554-1

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