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

• Main Authors: Yahya Benbouchta (Author), Nicole De Leeuw (Author), Saadia Amasdl (Author), Aziza Sbiti (Author), Dominique Smeets (Author), Khalid Sadki (Author), Abdelaziz Sefiani (Author)
• Format: Book
• Published: BMC, 2021-09-01T00:00:00Z.
• Subjects: article
• Online Access: Connect to this object online.

Abstract 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...