Hello,

I see you are asking "What are the symptoms for 1p36 deletion syndrome?"

1p36 deletion syndrome is a congenital genetic disorder characterized by moderate to severe intellectual disability, delayed growth, hypotonia, seizures, limited speech ability, malformations, hearing and vision impairment, and distinct facial features.

You can also visit this site - the mental health help center. com/condition/1p36-deletion-syndrome/c/8804

nondisjunction

Deletion Syndrome or Williams Syndrome

deletion syndrome is a disorder caused by the deletion of a small piece of chromosome 22. The deletion occurs near the middle of the chromosome at a location designated q11.2.

My son has 1p36 syndrome and has been to the dentist a few times. He is 4 years old and doesn't communicate very well. Luckily he goes to a pediatric dentist who is very understanding. For most of the visits they just have us hold him while they do a quick exam. He did have to have a filling once and they used a mouth piece to hold his mouth open and rolled him up in a blanket so he would stay still. He did cry the entire time but it only took a few minutes. Hope this helps.