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Article

A Case of Inherited t(4;10)(q26;q26.2) Chromosomal Translocation Elucidated by Multiple Chromosomal and Molecular Analyses. Case Report and Review of the Literature.

Genes - 7 Dec 2021

Popescu Roxana, Grămescu Mihaela, Caba Lavinia, Pânzaru Monica-Cristina, Butnariu Lăcrămioara, Braha Elena, Popa Setalia, Rusu Cristina, Cardos Georgeta, Zeleniuc Monica, Martiniuc Violeta, Gug Cristina, Păduraru Luminiţa, Stamatin Maria, Diaconu Carmen C, Gorduza Eusebiu Vlad

Abstract excerpt

We present a complex chromosomal anomaly identified using cytogenetic and molecular methods. The child was diagnosed during the neonatal period with a multiple congenital anomalies syndrome characterized by: flattened occipital region; slight turricephaly; tall and broad forehead; hypertelorism; deep-set eyes; down slanting and short palpebral fissures; epicanthic folds; prominent nose with wide root and bulbous...

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Share to Abnormalities, Multiple
Share to Chromosome Deletion

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosomes, Human, Pair 10

Share to Chromosomes, Human, Pair 4

Share to Infant, Newborn

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Share to Translocation, Genetic

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Source

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Identifiers

PMID: 34946906
DOI: 10.3390/genes12121957
PMCID: PMC8701147

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