I've name changed for this very specific question.
Has anyone had a experience of delayed fontanelle closure? My daughter is nearly 4. She's under the care of a paediatrician because of this. So far all tests have come back clear including blood tests, CT scan, and an xray which showed normal bone age.
They're doing some genetic tests. She is short (first centile) but she has no other physical features that would suggest a genetic condition.
Anyone else heard of a child with this?