Fig 3 - uploaded by Mohammadkazem Bakhshandeh
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Chromosome study of the patient on the basis of fluorescent in situ hybridization: Fluorescent in situ hybridization was performed on metaphase sreads using the cytocell prader-willi/Angelman (SNRPN/IC)probe. Conclussion:46XX,ish del(15)(q11q13)(SNRPN/IC)Compatible with prader-willi / Angelman syndrome.
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Objective
Angelman Syndrome (AS) is a genetically determined syndrome that has a unique behavioral phenotype. This syndrome is described as jerky ataxia and an unusual happy facial expression with pathological laughter. Severe mental retardation is a unique feature of the syndrome, together with microbrachycephaly and abnormal electroencephalograph...
