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

• Главные авторы: Yahya Benbouchta (Автор), Nicole De Leeuw (Автор), Saadia Amasdl (Автор), Aziza Sbiti (Автор), Dominique Smeets (Автор), Khalid Sadki (Автор), Abdelaziz Sefiani (Автор)
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• Опубликовано: BMC, 2021-09-01T00:00:00Z.
• Предметы: article
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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...