Genetic information
-It is a gene disorder.
-There is a nucleotide mutation in the LMNA gene, typically found on chromosome 1.
- It is autosomal dominant meaning you only need one allele to appear
-The substitution of (GGC to GGT) causes a mutated form of Lamin A.
- Normal Lamin A acts as supports to the nuclear envelope of a cell.

Definition: Progeria Syndrome is an extremely rare genetic disorder of unknown origin that manifests a premature aging in children.