15q26 deletion in a patient with congenital heart defect, growth restriction and intellectual disability: case report and literature review

BACKGROUND: 15q26 deletion is a relatively rare chromosomal disorder, and it is described only in few cases. Patients with this aberration show many signs and symptoms, particularly pre- and postnatal growth restriction, developmental delay, microcephaly, intellectual disability and various congenit...

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Detalles Bibliográficos
Autores principales: Benbouchta, Yahya, De Leeuw, Nicole, Amasdl, Saadia, Sbiti, Aziza, Smeets, Dominique, Sadki, Khalid, Sefiani, Abdelaziz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447573/
https://www.ncbi.nlm.nih.gov/pubmed/34530895
http://dx.doi.org/10.1186/s13052-021-01121-5

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8447573/
https://www.ncbi.nlm.nih.gov/pubmed/34530895
http://dx.doi.org/10.1186/s13052-021-01121-5

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