Article

15q26 Deletion in a Patient with Congenital Heart Defect, Growth Restriction and Intellectual Disability: Case Report and Literature Review

2020-10-30

Abstract excerpt

<h4>Background: </h4> 15q26 deletion is a relatively rare chromosomal disorder described in only few cases. Patients with this aberration display numerous symptoms particularly, pre- and postnatal growth restriction, microcephaly, intellectual disability, dysmorphic gestalt and various congenital malformations. Case presentation We report on a girl, four years old, of consanguineous parents, with a de novo 15q26 d...

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Literature Corpus work: 8dd74834-35a0-59a6-9a76-3f3d2dd1c4ef
DOI: 10.21203/rs.3.rs-34129/v2

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