Abstract
The Cri-Du-Chat Syndrome is a rare disease, characterized by cry like meow cat, mental retardation, microcephaly, ocular hypertelorism, hypotonia, palpebral antimongoloid resulting from deletion in a particular region of chromosome 5. The main of this project is to analyze the amino acid plasma profile of patients with Cri-Du-Chat Syndrome (SCDC), and compare with individuals do not carry…