Partial trisomy 19p13.3-p13.2 linked to microcephaly, hydronephrosis, and hearing loss in first Middle East case
Rare Chromosome Condition Linked to Developmental Delays
This case report and literature review describes a boy with a 6.8 Mb gain at chromosome 19p13.3-p13.2, inherited from a maternal balanced tr…
A boy with a rare extra piece of chromosome 19 had microcephaly, hearing loss, and kidney swelling, a new case report says.
