Chromosome 1p36 deletion syndrome detected by NGS
Watanabe, Miki Tokushima University
Ono, Akemi Tokushima University
Kohmoto, Tomohiro Tokushima University
Although chromosome 1p36 deletion syndrome is considered clinically recognizable based on characteristic features, the clinical manifestations of patients during infancy are often not consistent with those observed later in life. We report a 4-month-old girl who showed multiple congenital anomalies and developmental delay, but no clinical signs of syndromic disease caused by a terminal deletion in 1p36.32-p36.33 that was first identified by targeted-exome sequencing for molecular diagnosis.
Human Genome Variation
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