Trisomy 13

A birth defect that occurs when the child receives duplicated information from chromosome #13. This disorder affects approximately 1 in every 10,000 babies. Common symptoms of the disorder include cleft palate/cleft lip, close set or fused eyes (becoming a cyclops), low muscle tone, polydactyly, hernia, coloboma, severe mental retardation, undescen...
Found on
No exact match found