Microdeletion syndrome is a rare condition which can be diagnosed by
fluorescent in situ hybridization (FISH) method. We analyzed microdeletion
syndromes cases during ten years period (2005-2015) at The Hospital of
Lithuanian University of Health Sciences. We report 2 patients with
Prader-Willi syndrome, 2 patients with Smith-Magenis syndrome, 1 patient
with Angelman syndrome and 1 patient with Cri du Chat syndrome. All
syndromes were confirmed by FISH. These cases contain mainly data about
phenotype abnormalities and clinical symptoms.
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