hi, i hope no one minds me posting this here, i am not sure if this is the best place to put this thread.
i recently became aware what seems to be a strong family history of asd/autism. i am adopted and didn't have access to my history before. without going into massive detail, the links are close to me as the most affected people are my biological brother and first cousins on one side of my family. also, it can be traced back through 3 generations to my biological grandfather. only males appear to be affected.
i have a DD who is 21 months and a newborn DS.
assuming there is a hereditary component (or is there really?), what routine or special checks should i ensure they get to monitor their development? even if such tests did show the likelihood of their being asd, do early intervention therapies make any difference ?
i appreciate these are questions to which there is unlikely to be a clear answer or on which there may be differing views. i have this information about family history without a lot of the relevant context and would appreciate some thoughts on how to organise my thinking on this point esp if i need to be monitoring development particularly closely.
any guidance would be gratefully appreciated.