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- W2900705989 abstract "Interstitial deletions involving 6q25 are rare chromosomal abnormalities associated with distinctive phenotypic features. We describe a 9-year-old boy who was followed from his infancy due to his multiple congenital anomalies and complex medical history. Over the years, a number of diagnoses were considered including Cornelia de Lange syndrome, Rubinstein-Taybi syndrome, as well as “a novel genetic disorder.” Various genetic tests, including a BAC-based array-CGH analysis, were reported as normal. Recently, a SNP-based microarray analysis was performed and showed an 11.1-Mb deletion from 6q25.2 to 6q26, including <i>ARID1B </i>and<i> ZDHHC14</i>. Recent literature suggests that the 6q25 deletion syndrome is a recognizable entity characterized by growth delay, developmental disabilities, microcephaly, hearing loss, and variable other malformations including cleft palate. These features overlap with those of Coffin-Siris syndrome, which is caused by deletions and loss-of-function mutations of <i>ARID1B</i>. Retrospectively, this patient has features resembling both Coffin-Siris and 6q25 microdeletion syndromes." @default.
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- W2900705989 date "2018-01-01" @default.
- W2900705989 modified "2023-09-27" @default.
- W2900705989 title "Multiple Congenital Anomalies and Global Developmental Delay in a Patient with Interstitial 6q25.2q26 Deletion: A Diagnostic Odyssey" @default.
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- W2900705989 doi "https://doi.org/10.1159/000494871" @default.
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