Using Array-Based Comparative Genomic Hybridization to Diagnose Pallister-Killian Syndrome.
- Author:
Mi Na LEE
1
;
Jiwon LEE
;
Hee Joon YU
;
Jeehun LEE
;
Sun Hee KIM
Author Information
- Publication Type:Case Reports
- Keywords: Pallister-Killian syndrome; Isochromosome 12p; Tetrasomy 12p; Array CGH
- MeSH: Child, Preschool; Chromosome Disorders/*diagnosis; Chromosomes, Human, Pair 12; Comparative Genomic Hybridization; Female; Humans; In Situ Hybridization; Infant; Male; Tetrasomy
- From:Annals of Laboratory Medicine 2017;37(1):66-70
- CountryRepublic of Korea
- Language:English
- Abstract: Pallister-Killian syndrome (PKS) is a rare multisystem disorder characterized by isochromosome 12p and tissue-limited mosaic tetrasomy 12p. In this study, we diagnosed three pediatric patients who were suspicious of having PKS using array-based comparative genomic hybridization (array CGH) and FISH analyses performed on peripheral lymphocytes. Patients 1 and 2 presented with craniofacial dysmorphic features, hypotonia, and a developmental delay. Array CGH revealed two to three copies of 12p in patient 1 and three copies in patient 2. FISH analysis showed trisomy or tetrasomy 12p. Patient 3, who had clinical features comparable to those of patients 1 and 2, was diagnosed by using FISH analysis alone. Here, we report three patients with mosaic tetrasomy 12p. There have been only reported cases diagnosed by chromosome analysis and FISH analysis on skin fibroblast or amniotic fluid. To our knowledge, patient 1 was the first case diagnosed by using array CGH performed on peripheral lymphocytes in Korea.
