Open Access

A maternally inherited 8.05 Mb Xq21 deletion associated with Choroideremia, deafness, and mental retardation syndrome in a male patient

  • Siying Liang1,
  • Nan Jiang1,
  • Shuo Li1,
  • Xiaohu Jiang2 and
  • Dongyi Yu1Email author
Contributed equally
Molecular Cytogenetics201710:23

https://doi.org/10.1186/s13039-017-0324-6

Received: 3 January 2017

Accepted: 7 June 2017

Published: 14 June 2017

Abstract

Background

Deletions in Xq21 cause various congenital defects in males including choroideremia, deafness and mental retardation, depending on their size and gene content. Until now only a limited number of patients with Xq21 deletions has been reported.

Case presentation

Here we describe a 17-year-old male with choroideremia, deafness, and mental retardation syndrome. Using SNP arrays, an 8.05 Mb deletion in Xq21 was identified inherited from the apparently healthy mother. The deleted region harbors 12 OMIM genes, of which POU3F4, CHM, and ZNF711 might have contributed to the patient’s phenotype including hearing loss, poor vision, and intellectual disability. Moreover, the patient’s mother exhibits a normal phenotype while carrying the same deletion, which is often observed in previous studies on female carriers in families with this syndrome.

Conclusions

Our study confirms the causative effect between the Xq21 deletion in males and choroideremia, deafness and mental retardation.

Keywords

Xq21ChoroideremiaDeafnessMental retardationSNP arrays

Background

X-chromosome deletions can result in serious congenital defects. Males seldom exhibit these defects, as deletions on the X chromosome are essentially lethal in male embryos discarded at an early embryonic stage. Even though high-resolution SNP array analysis has been performed to identify small deletions on the X chromosome, the clinical significance of Xq21 deletions in males is still poorly understood. It has been shown that a contiguous gene Xq21 deletion, including POU3F4, CHM and ZNF711 genes, could result in choroideremia, deafness, and mental retardation syndrome. This deletion produces degeneration of the choriocapillaris, the retinal pigment epithelium, and the photoreceptor of the eye, as well as inner ear abnormality with progressive mixed hearing loss and intellectual disability. In the last decades, only six cases with Xq21 deletions have been reported [13]. Despite the severe symptoms exhibited by male probands, most female carriers are non-symptomatic or express only a mild phenotype [2].

Here we describe the case of a 17-year-old male with mental retardation, choroideremia, hearing impairment, cochlear deformity, and facial anomalies. Analysis by SNP array, identified an 8.05 Mb contiguous gene deletion in Xq21 harboring POU3F4, CYLC1, RPS6KA6, HDX, APOOL, SATL1, ZNF711, POF1B, CHM, DACH2, KLHL4, and CPXCR1 genes. The same deletion was identified in the apparently healthy mother. Our data contribute to further understanding the correlation between Xq21 deletions and the abnormal phenotypes. Furthermore, we present all the Xq21 deletion cases previously described in order to review the matter of genotype-phenotype correlations.

Case presentation

The patient was born by spontaneous delivery after an uneventful pregnancy (birth weight 3.350 kg and occipitofrontal circumference 35.5 cm) to phenotypically normal parents. He showed global development delay since infancy. He learned to speak at 18 months old and to walk at 2.5 years old. During childhood, he showed severe learning impairment and social disabilities. However, he was able to react to verbal words and to carry out brief communications. He has a narrow forehead, slightly drooping eyelids, short palpebral fissures, and prominent ears (Fig. 1). His IQ level is below 40, according to the Wechsler Intelligence Scale test, and his general cognitive ability is also low. His vision test result was out of the normal scale, indicating poor sight. His hearing test showed moderate hearing impairment with 60 dB of hearing loss. Ophthalmoscopy showed partial degeneration of the eye choroid (Fig. 2a). High resolution CT (HRCT) imaging showed that the base turn of the cochlea was shortened, the second turn and the apical turn were merged or unclearly divided, and the modiolus was absent, which evidently supported for the inner ear malformation (Fig. 2b). The patient’s mother also underwent the tests described above. However, her results were normal and there was no evidence suggesting that she might exhibit choroideremia, or hearing impairment in the future.
Fig. 1

Facial dysmorphism of the patient, including narrow forehead, slightly drooping eyelids, short palpebral fissures and prominent ears

Fig. 2

a Ophthalmoscopy photos of the patient showed the partial degeneration of the choroid in both eyes. b High-resolution CT imaging showed the cochlea deformity of the patient, including the short base turn of the cochlea, unclear division between the second turn and the apical turn of the cochlea and the absence of the modiolus

Methods

Peripheral blood samples of the patient and his mother were used for genomic DNA extraction. Briefly, genomic DNA was isolated from whole blood using DNA Blood Mini Kit (Qiagen, Germany). Chromosomal microarray analysis was performed using Cytoscan 750 K chip, (Affymetrix, USA) according to manufacturer’s instructions. CMA was performed with CytoScan 750 K array (Affymetrix, Santa Clara, CA, USA) according to the manufacturer’s recommendations. The platform is composed of 550,000 non-polymorphic CNV probes and more than 200,000 SNP probes with an average resolution of 100 kb. The data was analyzed using chromosome analysis software ChAS (Affymetrix, USA). Primers flanking the deleted fragment, POU3F4and CPXCR1, were designed using Primer 5.0 (Premier, Canada) and were used to validate the deletion by PCR and agarose electrophoresis. Data collection were performed via searching in DECIPHER database (https://decipher.sanger.ac.uk/) and ISCA (https://www.clinicalgenome.org/) in order to identify cases of patients carrying similar deletions [4].

Results

SNP array analysis detected an 8.05 Mb deletion in the long arm of the X chromosome at Xq21.1-21.31 (Fig. 3) in both the patient and his mother. The genomic position of this deletion according to GRCh37/hg19 was Chr X: 80,817,978-88,868,979. The deleted region harbors 12 genes, including POU3F4, CYLC1, RPS6KA6, HDX, APOOL, SATL1, ZNF711, POF1B, CHM, DACH2, KLHL4 and CPXCR1(Table 1). The PCR result confirmed the SNP array data.
Fig. 3

Detected by SNP arrays analysis, an 8.05 Mb deletion on the long arm of the X chromosome at Xq21 in the patient

Table 1

OMIM genes included in the deletion, protein products and function and disease caused

Gene

Protein

Protein function

Disease

POU3F4

POU class 3 homeobox 4

Inner ear development

Non-syndromic hearing loss

CYLC1

Cylicin, basic protein of sperm head cytoskeleton 1

Spermatid differentiation

None

RPS6KA6

Ribosomal protein S6 kinase A6

Activation of the mitogen-activated kinase cascade

None

HDX

Highly divergent homeobox

Unknown

None

APOOL

Apolipoprotein O like

Lipoprotein complexes circulation

None

SATL1

Spermidine/spermine N1-acetyl transferase-like 1

Unknown

None

ZNF711

Zinc finger protein 711

Similarity to protein that acts as a transcriptional activator

Mental retardation, X-linked type 97

POF1B

Premature ovarian failure, 1B

Germ cell division

Premature ovarian failure

CHM

Rab escort protein 1

Regulation of vesicular traffic

Choroideremia

DACH2

Dachshund family transcription factor 2

Regulation of organogenesis and myogenesis

None

KLHL4

Kelch like family member 4

Banding domain of actin

None

CPXCR1

CPX chromosome region, candidate 1

Contains a motif similar to motifs in zinc finger protein

None

Discussion

Patients with choroideremia, deafness, and mental retardation were first described by Ayazi [1]. In a kindred (XL-45), two brothers and their maternal uncle exhibited this syndrome, while the females had only characteristic retinal changes. The second kindred (XL-62) was reported by Nussbaum [2], in which two matrilineal first cousins had choroideremia, mental retardation, deafness, and short stature. Nussbaum found that affected members from both kindreds, XL-45 and XL-62, carried similar size deletions in Xq21. Following fine mapping studies revealed that the deleted region contained putative loci for choroideremia, X-linked deafness-2 (DFNX2), and non-specific X-linked mental retardation. These loci are currently known as genes CHM and POU3F4 [5]. Another case was reported by Song et al. [3], in which a 3-year-old boy showed deafness and mild mental retardation, while genetic analysis confirmed the presence of a 16 Mb Xq21 deletion. In this kindred (SV-08-20), the carrier mother had only mild high-tone hearing loss. To the best of our knowledge, so far, our patient is the seventh reported case with this syndrome. Although the genetic deletion and clinical phenotype are highly typical compared to the previous reports, there are still notable distinctions. For instance, in our case the patient’s mother exhibits no symptoms, which is consistent with most of the female carriers in XL-62 but not with those in XL-45. A detailed comparison of all the seven cases and female carriers is made in Table 2.
Table 2

Detailed comparison of the phenotype, the deleted region and the genes included in the probands and female carriers in the reported kindreds

Kindred

Phenotype of male patients

Phenotype of female carriers

Deleted region in Chr X

Refered OMIM genes

Reference

XL-45

Choroideremia, mental retardation, deafness

Retinal changes of choroiderenia

Between DXS232 and DXS95 (fine mapping) DXS232 and DXS95 DXS232 and DXS95

Not reported

Ayazi,1981

Nussbaum,1987

XL-62

Choroideremia, short stature, mental retardation, deafness

Mild high frequency sensorineural hearing loss (seen in only one out of four)

Between DXS72 and DXS214 (fine mapping) DXS232 and DXS95 DXS232 and DXS95

Not reported

Nussbaum, 1987

SV-08-20

Severe bilateral hearing loss, central hypotonia, developmental delay, mild mental retardation, vesicoureteral reflux

Mild high-tone hearing loss

16 Mb Xq21 (estimated by PCR)

POU3F4, CHM

Song, 2010

Present case

Choroideremia, mental retardation, hearing impairments, cochlea deformity, facial anomalies

Normal

8.05 Mb Xq21 Chr X: (80,817,978-88,868,979)

CHM, POU3F4, ZNF711, POF1b

-

As deafness and choroideremia are commonly observed in all the recorded cases, POU3F4 and CHM gene deletions are two basic indexes for diagnosis. POU3F4 gene encodes POU-III class factor 4, a transcription factor that mediates epigenetic signals, which induce striatal neuron-precursor differentiation. By generating non-functional products, mutations in this gene often lead to DFNX2, which is characterized by conductive and sensorineural progressive hearing loss and pathognomonic temporal bone deformity, including dilatation of the inner auditory canal and fistulous connection between the internal dilatation auditory canal and the cochlear basal turn [6]. Accordingly, our patient showed inner ear deformity with short base turn of the cochlea, unclear division within the cochlea and the absence of the modiolus, which is a typical consequence of POU3F4 deletion.

CHM gene defect is a confirmed cause of choroideremia, an X-linked disease leading to progressive vision loss. CHM encodes REP1, a subunit of geranylgeranyl transferase that affects the regulation of vesicular traffic. Deletions and point mutations in CHM generate a truncated product and result in degeneration of the choriocapillaris, retinal pigment epithelium, and eye photoreceptors [7]. Despite the strong pathogenicity in male patients, mutations in CHM do not have the same effect on female carriers. This might be a consequence of the non-random inactivation of the X chromosome, which has been validated by Carrel and Willard in their studies on CHM-inactivation escaping pattern [8].

Notably in previous reports, all male probands exhibited prominent phenotypes, including both choroideremia and hearing impairment, while the female carriers of each kindred exhibited only one of the clinical characteristics and their symptoms were milder. In our case, the mother manifests no symptoms, similar to the female carriers in kindred XL-62. This diversity of female carrier’s phenotypes shows that although a regressive inheritance pattern is clear, the exact influence of gene loss towards female carriers is still unpredictable.

ZNF711 is a member of the zinc-finger gene family. It has been proved that the ZNF711 protein interacts, as a cofactor, with demethylase PHF8 in binding to target genes, thus suggesting a role for ZNF711 in transcriptional modulation [9]. Although limited in clinical case reports, ZNF711 gene loss is believed to be causative to non-specific X-linked mental retardation(MRX97). By exon sequencing of the X chromosome in 208 families with X-linked mental retardation, Tarpey et al. 2009. identified two truncating mutations of ZNF711 in two families with MRX97 [10]. Clinical reports of sporadic cases also support this pathogenetic connection [11]. Recently in 11 male patients from two new found MRX97 families, Van der Welf et al. [12] identified a frameshift deletion and a missence mutation in ZNF711 which both predict the deleterious effect and cause the disease. By expression analysis of cell culture, they also showed that these mutations induced differential expression of genes known to be expressed in the brain compared to controls, which adds evidence to ZNF711 as a transcription factor. In our case, our patient exhibits severe intellectual disabilities and facial dysmorphism, which are coincided with the phenotype of MRX97. Considering of other pathogenetic genes (POU3F4 and CHM) have no independent effect to mental retardation, ZNF711 loss may have contributed majorly to the MRX97 phenotype of our patient.

We continued to search in the Decipher and ISCA databases for similar size deletions at Xq21.1 and identified 11 deletions with certain pathogenicity. Although most of them have concurrent phenotypes, none is exactly corresponds to the phenotypes of our patient. A notable fact is that deletions which does not contain ZNF711 are often not associated with mental retardations (Decipher 289,263, 287,836, ISCA 582602, 3,442,681, and 578,452, Fig. 4) or only with moderate MD (Decipher 287,069, Fig. 4). This furtherly suggests that ZNF711 gene loss might be an independent cause to mental retardation.
Fig. 4

Xq21.1 deletion. The upper part of the figure illustrates the exact locations of the protein coding genes included in this region. The lower part of the figure schematically represents the Xq21.1 deleted region in our patient(in red) and other deletions reported in the Decipher(in black) and ISCA database(in red). The ID of each patient is reported. The clinical features of the patients are reported in parentheses below the corresponding deletion as described in Decipher (https://decipher.sanger.ac.uk/) and ISCA (https://www.clinicalgenome.org/)

Conclusion

In conclusion, our male patient carrying the 8.05 Mb Xq21 deletion exhibits a typical phenotype of choroideremia, deafness, and mental retardation syndrome, an association which has been demonstrated by previous cases. Meanwhile, as it is commonly observed in other female carriers, the mother of our patient, who carries the same deletion, is non-symptomatic. Additionally, comparing to previous reports our patient has a more compact deleted genome region which contains less OMIM genes. This may help to prune down the causative genes of disease phenotypes. Although our study confirms the causative effect of the Xq21 deletion in males with multiple congenital defects, more cases are needed to be studied in order to clarify the consequences of gene loss in this chromosomal region and the effects on the phenotype.

Abbreviation

APOOL

Apolipoprotein O like

ChAS: 

Chromosome analysis suite (Affymetrix)

CHM

Rab escort protein 1

Chr: 

Chromosome

CPXCR1: 

CPX chromosome region, candidate 1

CYLC1

Cylicin, basic protein of sperm head cytoskeleton 1

DACH2

Dachshund family transcription factor 2

DFNX2: 

Deafness, X-linked 2

HDX: 

Highly divergent homeobox

HRCT: 

High-resolution computed tomography

IQ: 

Intelligence quotient

KLHL4: 

Kelch like family member 4

OMIM: 

Online Mendelian inheritance in man

PCR: 

Polymerase chain reaction

POF1B

Premature ovarian failure, 1B

POU3F4

POU class 3 homeobox 4

RPS6KA6

Ribosomal protein S6 kinase A6

SATL1

Spermidine/spermine N1-acetyl transferase-like 1

SNP: 

Single-nucleotide polymorphism

Xq21: 

X chromosome long arm q band 21

ZNF711

Zinc finger protein 711

Declarations

Acknowledgments

We thank the patient and his family for their participation in this study.

Funding

Not applicable.

Availability of data and materials

Please contact author for data requests.

Authors’ contributions

By carrying out molecular genetic tests, helping in the clinical examination of the patient and writing manuscript, Siying L,NJ and Shuo.L have contributed equally to this articles. XJ helped in data research for revision. DY conceived of the study and helped to draft the manuscript. All authors read and approved the final manuscript.

Competing interests

The authors declare that they have no competing interests.

Consent for publication

The legal guardian of the patient has authorized the usage of patient’s data(including facial images) for publication. See supplementary material.

Ethics approval and consent to participate

This study has been approved by the Ethic Committee of Qingdao Women and Children’s hospital, and with full knowledge, the legal guardian of the patient has signed written informed consent to participate in it.

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Authors’ Affiliations

(1)
Genetic Testing Center, Qingdao Women and Children’s Hospital, Qingdao University
(2)
Qingdao Women and Children’s Hospital, Qingdao University

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Copyright

© The Author(s). 2017

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