Individuals with tuberous sclerosis have a mutation in either the gene TSC1 or TSC2, and these mutations have an autosomal dominant inheritance pattern.
Symptoms of tuberous sclerosis are often related to the hamartomas in the brain which cause problems like seizures, learning difficulties, and cognitive deficits.
These developmental masses happen frequently in patients that also have tuberous sclerosis —a genetic disorder causing these non-cancerous masses to form in various tissues.
The ships are slightly longer and slightly wider due to the tuberous bow stem, and on the expanded ship, one more row of containers can be stacked from head to toe on both sides.