A Pilot Study about Clinical Features of Aberrations Chromosome 22q

Abstract Objective A significant number of genetic variations have been identified in chromosome 22, using molecular genetic techniques. Various genomic disorders on chromosome 22, including cat's eye syndrome caused by extra copies of the proximal region of the 22q chromosome, are now well-defined. Our aim in the study was to show phenotypic variability associated with rearrangements of the 22q chromosomal region. Methods We focused our study on clinical aspects of these disorders, including genetic testing, genotype-phenotype correlation, and potential treatments. A total of 998 patients were referred for genetic analysis (Karyotyping, MLPA, array-CGH) during January 2015 to February 2020 because of intellectual deficiency, behavior issues, and/or multiple congenital abnormalities in several genetics departments. Informed consent was obtained from all the patients and/or their parents. Results 22q11.21 or 22q13.33 microdeletions and 22q11.22-q11.23 microduplication were identified in 31 patients out of referrals. The 22q aberrations were detected in 31/998 patients, giving a prevalence of 3.1%. In this study, 18 patients with 22q11.2 (LCR22A-H) deletion, three patients with 22q13.31 deletion, 9 patients with 22q11.2 duplication and one patient with 22q13.31 duplication were identified. We report on the clinical and molecular characterization of 31 individuals with distal deletions and duplications of chromosome 22q. Conclusions The current study demonstrated in the largest postnatal case series reporting the whole spectrum of atypical phenotypic and genotypic variations at 22q. We believe that when all the phenotypic differences are taken into account, various anomalies including developmental delay and intellectual disability might be considered as an indication to search for aberrations of 22q along with congenital heart diseases.

Introduction approximately 51 million base pairs, with more than 855 annotated genes. 1,2 A significant number of genetic variations have been identified in chromosome 22, using molecular genetic techniques. Nonmosaic trisomy and monosomy of chromosome 22 are observed in the prenatal period. Trisomy 22 is the second aneuploidy after trisomy 16 in spontaneous abortions, seen in approximately 2 to 5% of cases. 3 While most of these disorders are rare, the prevalence of some, such as velocardiofacial syndrome (also known as VCFS, 22q11 deletion syndrome, and DiGeorge syndrome [DGS]), is as common as 1: 2000 people. Various genomic disorders on chromosome 22, including cat's eye syndrome caused by extra copies of the proximal region of the 22q chromosome, are now well-defined (►Table 1). Cat's eye syndrome caused by extra copies of the proximal region of the 22q chromosome, VCFS, 22q11.2 duplication syndrome, 22q11.2 deletion syndrome, supernumerary der (22) t (11; 22), 3: 1 caused by malsegregation of the t (11; 22) syndrome, and 22q13.3 deletion syndrome are better defined today (►Table 1). 4 In addition to the genomic disorders with molecular causes listed in ►Table 1, there are hundreds of disorders associated with a gene, but the underlying cause is unknown or the disturbances are determined by statistical methods. Pathogenic copy number variants (CNVs) and CNVs of unknown clinical significance have been identified and added to the genetic variations to the complexity of human diseases. 5 The definition of the proximal region of chromosome 22q11.2 illustrates such progress.
This genomic region is rich in low copy repeats (LCRs), including LCR22A to LCR22H. Most of the genomic abnormalities of chromosome 22 occur as a result of LCR-mediated nonallelic homologous misalignments and intrachromosomal or interchromosome unequal recombination (NAHR) during meiosis. 6 In addition to the commonly deleted/duplicated region (LCRs A to D surrounded by LCR22s at both proximal and distal cutpoints for 3 Mb, 22q11.2 deletions and duplications), several "non-standard" deletions/duplication with var-iable breakpoints results from differential recombination from LCR22A to LCR22H (►Fig. 1). Some of these have been identified as separate deletion/duplication syndromes with varying genomic dimensions such as 22q11.2 distal deletion syndrome and 22q11.2 distal duplication syndrome. 7,8 In addition to the LCR-mediated NAHR mechanism, several other mechanisms have been proposed to explain the formation of CNVs in the human genome, including CNVs on chromosome 22 such as nonhomologous splicing, microhomology-mediated break-induced replication, and tandem repeats-mediated genomic rearrangement. Correct determination of the breakpoints of a CNV is a prerequisite for understanding the basic mechanisms that lead to its formation and establish CNV-phenotype correlation.
Our aim in the study is to show phenotypic variability associated with rearrangements of the 22q11.2 chromosomal region.
We focus our study on clinical aspects of these disorders, including genetic testing, genotype-phenotype correlation, and potential treatments.

Materials and Methods
All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee (TUMF Scientific Research Ethics Committee Directive) and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards.
A total of 998 patients were referred for genetic analysis during January 2015 to February 2020 because of intellectual deficiency, behavior issues, and/or multiple congenital abnormalities in several genetics departments. Informed consent was obtained from all the patients and/or their parents. 22q11.21 or 22q13.33 microdeletions and 22q11.22-q11.23 microduplication were identified in 31 patients out of referrals. The clinical data of the 31 patients were retrospectively

Karyotype and FISH
Patients were referred for cytogenetic testing. Cytogenetic analysis on cultured blood lymphocytes was performed, according to standard protocols. Trypsin-Leishman G banded (GTL) metaphases were interpreted at a resolution level of 450 bands.

MLPA
Multiplex ligation-dependent probe amplification was performed on DNA from peripheral blood lymphocytes. Kits P023B, P250 and P324-A1 for DGS/VCFS/CES (MRC-Holland, Amsterdam, Netherlands) were used. The three kits test 65 loci on 22q11 (8 on the CES region, 37 within the TDR and 20 adjacent distal to the TDR), 2 on 22q13, 7 on 4q, 1 on 7p, 5 on 8p, 2 on 9q, 9 on 10p, 1 on 10q, 6 on 17p, and 2 on 18q, most of them involved in the phenotypes of DGS and VCFS. Data analysis was made against up to five control samples using the MRC Coffalyser v8 and v9 softwares (MRC-Holland) or an in-house Excel spreadsheet.
Genomic DNA was extracted from the patients' peripheral lymphocytes using the QIAamp DNA Blood Midi kit (Qiagen, Valencia, CA). DNA concentration was determined with Nano-Drop ND-1000 spectrophotometer and software (NanoDrop Technologies, Berlin, Germany). Pathogenic CNVs were identified by CMA, using a 180 K CGH þ SNP (ISCA design, Agilent, Santa Clara, CA) array, as part of the clinical testing for congenital anomalies, neurodevelopmental problems, and abnormal fetal ultrasound. Image was analyzed using CytoGenomics 2.7 software (Agilent Technologies, Santa Clara, CA, United States).
Validation of the microdeletion detected by array CGH was validated by fluorescence in situ hybridization. Fluorescence in situ hybridization (FISH) on metaphase spreads with probes for the DiGeorge critical region (D22S553, D22S942) as well as control probes for a more distal region on 22q13.3 (arylsulfatase A, LSI, ARSA, all from Vysis, Downers Groove, United States)

Statistical Analysis
We performed one-tailed Chi-square tests and calculated p values at the 95% confidence level to determine the differences in proportion of observed cases between male and female patients. The proportion of cytogenetic abnormalities was expected to be equal (50% each) between males and females. Variables, presented as a percentage normalized to the total number of male or female patients, were compared. Findings with p < 0.05 values were accepted as statistically significant.

Results
All patients had been referred for diagnostic testing by aCGH as part of standard clinical diagnostic workup. The 22q aberrations were detected in 31/998 patients, giving a prevalence of 3,1%. The patient cohort consisted predominantly of pediatric patients, with ages ranging from 5 days to 42 years, (mean¼ 9.9 years, median ¼ 5 years). Although gender biases for other susceptibility CNVs such as 16p13.11 have been reported in different studies 9 , the sex ratio here was equivalent for patients (16 females, 15 males). Phenotypic details of the patients were ascertained first from the referral information provided prior to testing, and then by interrogation of patient notes and letters to the referring consultants, requesting detailed clinical information. Details of patients and clinical findings are provided in ►Table 2.
The phenotypes of the cases are summarized in ►Table 2. The clinical phenotype varied among the individuals in this study, although a majority of cases displayed various degrees of developmental delay, ranging from mild to severe, and speech disturbances. Other clinical features present in more than five cases included behavioral problems, hypotonia, and dysmorphic facial features.

Discussion
In the present study, we report on the clinical and molecular characterization of 31 individuals with distal deletions and duplications of chromosome 22q. We detected 22q11.2 duplications in 9 patients and 22q13.31 duplications in one patient. Among the 998 patients tested, the estimated frequency of 22q11 and 22q13 duplications were approximately 1,002%. The estimated frequency in our patient population is slightly higher compared with the studies of Coppinger et al, who identified 18 distal duplications among 22,096 patients tested, and Wincent et al, who identified 16 distal duplications among 11,463 patients. Since a patient group with speech delay, brain malformations, and autism spectrum disorders was included in our study, this may have resulted from patient selection. [8][9][10] There is no standard procedure for screening for duplication in 22q11.2, because these patients show different clinical manifestations, only some of which are compatible with 22q11.2 deletion syndrome, usually in a milder phenotype. [11][12][13][14] Because the entire clinical spectrum is still unknown and most of these individuals overlap with normality, finding correlations of the sizes and positions of these duplications and phenotype is more difficult than deletions. 12,13 Deletions at 22q11.2 had a standard 3 Mb deletion in 87% of cases, a smaller, proximally nested 1.5 Mb deletion in 7% of cases, and other atypical deletions, nested, overlapping, or typically deleted region (TDR) clustered together. By NAHR after asynchronous replication, large low-copy repeats at 22q11,2 (LCR22s A to D) mediate repetitive deletions, while smaller LCRs (E-H) alongside recently described uncommon deletions or alternate breakpoints. 6,[15][16][17][18] In this paper, we present nine patients referred to us for genetic diagnosis of 22q11.2 deletion syndrome. We discuss screening diagnostic strategies for patients referred for the 22q11.2 deletion test as well as the clinical implications of these findings for a potential genotype-phenotype correlation.
The chromosome region 22q11.2 has long been recognized as a hotspot for genomic rearrangement and related disorders such as 22q11.2 deletion syndrome (DGS/VCFS, OMIM 188400/OMIM 192430), der(22) t(11; 22) syndrome (OMIM 609029), and cat-eye syndrome (OMIM 115470). Der (22) syndrome and cat eye syndrome are rare conditions characterized by an increased copy number of the most centromeric portion of 22q11, whereas 22q11.2 microdeletions are more common with an estimated frequency of 1 in 4,000 to 6,000 live births. 19,20 22q11 deletion syndrome is characterized by not only congenital heart defects, immunodeficiency, transient neonatal hypocalcemia, velopharyngeal insufficiency and a distinctive facial appearance but also learning disabilities and behavioral abnormalities. Phenotype varies with involvement of multiple organ systems. 5,21,22 The entire phenotypic spectrum of 22q11.2 deletion syndrome is provided by multiple dose-sensitive genes required for normal development across the 22q11.2 region. 23 Furthermore, nonoverlapping, atypical deletions have significantly overlapping phenotypes, suggesting several candidate genes for the syndrome, a common developmental pathway, or a positional gene effect at 22q11.2. [24][25][26][27][28][29] It has also been suggested that phenotypes represented by identical deletions at 22q11.2 are altered by parental imprinting, unbalanced regulatory effects, polymorphisms not masked by recessive mutations or hemizygosity, environmental factors, or stochastic events during morphogenesis. [29][30][31][32] Susceptibility to other syndromes has also been suggested in patients with the 22q11.2 deletion. 28,33,34 Several studies have identified several candidate genes at 22q11.2 that reproduce part of the phenotype or are suspected to alter disease susceptibility in animal models. 24,25,35,36 Accordingly, correlations made within a contiguous gene syndrome will always be subject to phenotype exclusions.
In the present study, of the 18 patients carrying 22q11.2 (LCR22A-H) deletion, most of the deletions were spread in the region between LCRB and E. The clinical findings of patients with this deletion showed a wide spectrum (►Table 2). The reason for the wide phenotypic variation is unknown, but possible explanations may be that the 22q11.2 deletion syndrome phenotype may be due to other genetic mutations or that other genes not involved in duplication may compensate or hinder the pathogenesis of duplication. However, a milder phenotype was observed in 22q11 duplication carriers (►Fig. 2). Duplication of chromosome 22q11 is also characterized by highly variable features, which may range from normal to mild and may include intellectual disability or learning disabilities, growth retardation, hypotonia, and delayed psychomotor development. 37,38 The most frequently reported symptoms in the 22q11.2 duplication syndrome are mental retardation/learning difficulties (cognitive deficits such as deficits of memory performance, perceptual organization and verbal comprehension, ADHD and speech impairment) (97%), delayed psychomotor development (67%), growth retardation (63%), and muscular hypotonia (43%). The most common dysmorphic features detected are hypertelorism (70%), broad flat nose (53%), micrognathia (52%), velopharyngeal insufficiency (48%), dysplastic ears (45%), epicanthal folds (42%), and downslanting palpebral fissures (41%). Other reported symptoms are congenital heart malformation, visual and hearing impairment, seizures, microcephaly, ptosis, and urogenital abnormalities. 14 In our patient group, changes covering the 22q13 band region (3 deletions and 1 duplication) were detected in four of our patients (►Table 2). Clinical findings in our patients with deletion including 22q13.33 region are hypotonia and motor retardation. This region has been associated with Phelan-McDermid syndrome (PMS) (phenotype MIM number: 606232) in the literature. PMS is a developmental disorder with variable features. Common features include neonatal hypotonia, global developmental delay, normal to accelerated growth, absent to severely delayed speech, autistic behavior, and minor dysmorphic features. The responsible gene SHANK3 is located in this region. [39][40][41] Duplication was detected in 22q13.33 region in one of our patients. A 3-yearold patient had clinical findings of flattened nasal root, stuttering, and craniosynostosis (►Table 2). In duplication, it included the SHANK3 gene as in deletions of the same region. On the basis of the phenotype of SHANK3-overexpressing mice, Han et al hypothesized that SHANK3 overexpression may have a role in hyperkinetic neuropsychiatric disorders in humans. 42 Duplication of the 22q13 region is included in the literature as chromosome 22q13 duplication syndrome (phenotype MIM number: 615538).
A larger deletion was detected in the 22q13.2q13.33 region of approximately 7.5 Mb in one of our patients. Although the deletion of the patient corresponded to the PMS syndrome region, it was observed that it spreads beyond this area. For instance, neonatal hypotonia and late walking were reported in 20% of those with deletions of just 22q13.33, yet were reported for more than 90% of those with the largest deletions (22q13.2). The traditional approach would ignore the difference in frequency and identify 22q13.33 as being the only candidate region. 43 Isolated motor retardation was found in the clinical findings of our patient.
The current study demonstrated in the largest postnatal case series reporting the whole spectrum of atypical phenotypic and genotypic variations at 22q. The knowledge regarding the distribution of findings within and associated with various organ systems may enable a rapid and precise diagnostic process. We believe that when all the phenotypic 22q Aberrations Atli et al. differences are taken into account, various anomalies including developmental delay and intellectual disability might be considered as an indication to search for aberrations of 22q along with congenital heart diseases. All of this data will contribute to the establishment of the true prevalence of these anomalies and defects, and reveal the importance of the multidisciplinary counseling and the contribution of this condition to positive outcomes.

Funding
None.