Please use this identifier to cite or link to this item: http://repositorio.unifesp.br/handle/11600/37916
Title: Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion
Authors: Guilherme, Roberta Santos [UNIFESP]
Soares, Karina Cunha
Simioni, Milena
Vieira, Tarsis Paiva
Gil-da-Silva-Lopes, Vera Lucia
Kim, Chong Ae
Brunoni, Decio [UNIFESP]
Spinner, Nancy Bettina
Conlin, Laura Kathleen
Christofolini, Denise Maria
Kulikowski, Leslie Domenici
Steiner, Carlos Eduardo
Melaragno, Maria Isabel [UNIFESP]
Universidade Federal de São Paulo (UNIFESP)
Universidade Estadual de Campinas (UNICAMP)
Univ Penn
Universidade de São Paulo (USP)
Keywords: ring chromosome 22
22q11
2 deletion
22q13 deletion
speech delay and SNP array
Issue Date: 1-Jul-2014
Publisher: Wiley-Blackwell
Citation: American Journal of Medical Genetics Part A. Hoboken: Wiley-Blackwell, v. 164, n. 7, p. 1659-1665, 2014.
Abstract: We report here on six patients with a ring chromosome 22 and the range of cytogenetic and phenotypic features presented by them. Genomic analysis was carried out using classical and molecular cytogenetics, MLPA (Multiplex Ligation-dependent Probe Amplification) and genome-wide SNP-array analysis. the ring was found in all patients, but Patient 6 displayed constitutional mosaicism with a normal cell line. Five patients had deletions in the ring chromosome 22, and in four of them the breakpointsunique for each patientcould be identified by genome-wide SNP-array analysis. One patient presented with a 22q11.2 deletion concomitant with the deletion caused by the ring formation. Common phenotypic features included autism, speech delay and seizures, as previously reported for individuals with r(22) and/or 22q13.3 deletions. Investigation of the genes within the deletions revealed multiple genes related to development of the central nervous system, psychomotor delay, severe language impairment, hypotonia, and autistic symptoms. There was no clear correlation between the severity of clinical features and the size of the deleted segment. This study underscores the variability in ring structure and clinical presentation of the r(22) and adds information to the limited literature on this rare disorder. (c) 2014 Wiley Periodicals, Inc.
URI: http://repositorio.unifesp.br/handle/11600/37916
ISSN: 1552-4825
Other Identifiers: http://dx.doi.org/10.1002/ajmg.a.36512
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