Interstitial deletion of the long arm of chromosome 3, del (3) (q25-q27), in association with Dandy Walker malformation: A case report

Interstitial deletions of the long arm of chromosome 3 are rare, and detailed genotype-phenotype correlations are not well established. The Dandy-Walker malformation (DWM) is one of the most common congenital cerebellar defects and can be associated with multiple congenital anomalies and chromosomal syndromes. We report an interstitial deletion of 3q: 46, XY, del (3) (q25; q27) in a Three-month-old boy with dysmorphic features, developmental delay, and a Dandy Walker malformation observed in MRI.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2024-09-30
DOI
https://doi.org/10.5281/zenodo.14964336
Primary Topic
Fetal and Pediatric Neurological Disorders
Type
article
Field-Weighted Citation Impact
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article

Interstitial deletion of the long arm of chromosome 3, del (3) (q25-q27), in association with Dandy Walker malformation: A case report

Zenodo (CERN European Organization for Nuclear Research)
Fetal and Pediatric Neurological Disorders
article

Interstitial deletion of the long arm of chromosome 3, del (3) (q25-q27), in association with Dandy Walker malformation: A case report

article en

Abstract

Interstitial deletions of the long arm of chromosome 3 are rare, and detailed genotype-phenotype correlations are not well established. The Dandy-Walker malformation (DWM) is one of the most common congenital cerebellar defects and can be associated with multiple congenital anomalies and chromosomal syndromes. We report an interstitial deletion of 3q: 46, XY, del (3) (q25; q27) in a Three-month-old boy with dysmorphic features, developmental delay, and a Dandy Walker malformation observed in MRI.

Zenodo (CERN European Organization for Nuclear Research)
Mohammed V University (MA)
Openalex Percentile: Top 39%
Fetal and Pediatric Neurological Disorders
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