A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome

Mutations in the Forkhead Box C1 (FOXC1) are known to cause autosomal dominant hereditary Axenfeld-Rieger syndrome, which is a genetic disorder characterized by ocular and systemic features including glaucoma, variable dental defects, craniofacial dysmorphism and hearing loss. Due to late-onset of ocular disorders and lack of typical presentation, clinical diagnosis presents a huge challenge. In this study, we described a pathogenic in-frame variant in FOXC1 in one 5-year-old boy who is presented with hypertelorism, pupil deformation in both eyes, conductive hearing loss, and dental defects. By whole exome sequencing, we identified a 3 bp deletion in FOXC1, c.516_518delGCG (p.Arg173del) as the disease-causing variant, which was de novo and not detected in the parents, and could be classified as a “pathogenic variant” according to the American College of Medical Genetics and Genomics guidelines. After confirmation of this FOXC1 variant, clinical data on Axenfeld-Rieger syndrome-associated clinical features were collected and analyzed. Furthermore, Although the affected individual present hearing loss, however, the hearing loss is conductive and is reversible during the follow-up, which might not linke to the FOXC1 variant and is coincidental. Routine examination of FOXC1 is necessary for the genetic diagnosis of hypertelorism-associated syndrome. These findings may assist clinicians in reaching correct clinical and molecular diagnoses, and providing appropriate genetic counseling. Supplementary Information The online version contains supplementary material available at 10.1186/s12920-021-01130-7.


Introduction
Axenfeld-Rieger syndrome (ARS) [MIM #602482] is an autosomal dominant disorder which is characterized by ocular and systemic features of variable degrees. ARS is a rare disorder, with prevalence estimated at 1 in 50,000 to 100,000 newborns. Patients with ARS present with ocular malformations particularly in the iris, cornea and the chamber angle, which belongs to the anterior segment of the eye. The presence of anomalies in the anterior chamber angle and drainage structure of the eye contributes to lifetime risk of developing glaucoma and can lead to irreversible blindness. Approximately 50% of ARS patients will develop into glaucoma, with an age of onset ranging from birth to late in adulthood [1,2]. Onset of glaucoma typically occurs before the teenage years [3].
In addition to the ocular features, ARS may have systemic abnormalities including craniofacial hypoplasia, dental and umbilical anomalies, cardiac defects, and hearing loss [4][5][6]. The most characterized systemic features are mild craniofacial dysmorphism, dental anomalies, and redundancy of periumbilical skin. Craniofacial features can be helpful in suggesting a diagnosis of ARS, particularly in family members with a mild ocular phenotype. Craniofacial features associated with ARS include a prominent forehead, hypertelorism, maxillary hypoplasia, and a flattened mid-face with a broad, flat nasal bridge, thin upper lip, and protruding lower lip. Dental anomalies include microdontia (small teeth), cone-shaped teeth, or fewer teeth than normal [7,8]. Additional noncommon features of ARS include pituitary abnormalities, hearing loss, kidney abnormalities, cardiovascular outflow tract malformation, and variable neurological and skeletal anomalies.
Disease heterogeneity has been generally recognized as the important challenge in diagnosis of ARS. The underlying genetic defects of ARS in 40% of patients is pathogenic variants in forkhead box C1 (FOXC1, MIM 601,090) or pituitary homeobox 2 (PITX2, MIM 601,542) [9,10], which both have important roles in embryonic development and regulate downstream genes which are important for cell differentiation and migration via DNA binding [11]. FOXC1 belongs to the FOX protein family, which are characterized by a winged helix DNA-binding domain [12]. Pathogenic variants in FOXC1 correlate with anterior segment dysgenesis 3 and ARS.
To date, there have been a few cases of FOXC1-associated ARS described in the Chinese population [13][14][15]. We report on one 5-year-old Chinese boy with hypertelorism, conductive hearing loss, dental defects and pupillary deformation, not the core features of ARS and identified heterozygosity for a de novo deletion in the FOXC1 gene by whole exome sequencing. This young boy was diagnosed with ARS via identification of this de novo variant in FOXC1. We also reviewed the literatures for cases of FOXC1-associated ARS.

Clinical evaluation
A 5-year-old boy was admitted to the Department of Otolaryngology, the PLA Rocket Force Characteristic Medical Center (Beijing, China). His parents complained hearing loss, small teeth and hypertelorism of this affected boy. The study was approved by the PLA Rocket Force Characteristic Medical Center Ethics Committees. Clinical information was gathered through multiple interviews. Physical examination, otoscopy, pure tone audiometric examination, best corrected visual acuity (BCVA), slit-lamp examination, intraocular pressure (IOP) measurement and fundus examination by indirect ophthalmoscopy were performed on the patient. Cardiac structure and function were evaluated by ECG and color Doppler echocardiography. In addition, serum chemistry analysis, blood count, urinalysis, and chest X-ray were performed in the patient.

Whole exome sequencing (WES) and bioinformatic analysis
WES genetic analysis were designed on offspring-parents trios, including one affected individual (II:1) and two unaffected parents (I:1 and I:2). Genomic DNA was extracted from peripheral blood using a blood DNA extraction kit according to the manufacturer's instructions (TianGen, Beijing, China). DNA was sheared, ligated to adaptors, extracted, amplified by ligationmediated PCR. 1 μg DNA library was mixed with Buffer BL and GenCap probe (MyGenostics, Beijing, China) for enrichment. Each captured library was loaded onto the Illumina NovaSeq 6000 platform. After filtering out low-quality and duplicate reads, clean data were aligned to the human reference genome hg19 using the Burrows-Wheeler Aligner. After alignment, variants were called using four types of software (SOAPsnp, GATK, Samtools and Platypus), merged into variant call format files and annotated by ANNOVAR and associated with multiple databases, including those with minor allele frequencies (MAF < 0.05), in public databases, including gnomAD, Inhouse database (MyGenostics), HGMD, and predicted by SIFT, PolyPhen-2, Mutation-Taster, GERP + + . Under the assumption of an autosomal-recessive or autosomal-dominant (de novo) pattern of inheritance, only variants that were homozygous or compound heterozygous in the affected boy and heterozygous in their parents, and de novo variant were selected as candidates. VarSome was used for a comprehensive interpretation of the variants [16]. Manually classification of those variants was conducted based on American College of Medical Genetics and Genomics (ACMG)/Association for Molecular Pathology (AMP) guidelines for genetic hearing loss [17]. Potential pathogenic variants finally screened by these analyses were confirmed using Sanger sequencing.

Clinical evaluations
We have clinically examined one affected boy (II:1) and his unaffected parents from this family (I:1 and I:2). The family pedigree is presented in Fig. 1a, and a summary of the main clinical characteristics is presented in comparison of those cases reported thus far (Table 1).
Detailed ocular analysis and auditory function was performed in the affected boy II:1. Although sensorineural hearing loss has been usually reported in FOXC1-related disease, conductive hearing loss induced by otitis media with effusion was identified in this patient, which is in accordance with observation of the pure tone hearing test, temporal bone CT and hearing recovery after 3 months (Fig. 1c). Craniofacial features observed in the proband include midface hypoplasia, hypertelorism (Fig. 1d). Dental examination showed microdontia (small teeth), cone-shaped teeth, and fewer teeth than normal (Fig. 1e). The best-corrected visual acuity was 20/20 in both eyes (OU). The intraocular pressure (IOP) was normal, of which 11 mmHg in the right eye and 10 mmHg in the left eye. Slit-lamp examination revealed pupillary deformation (corectopia) in OU (Fig. 1f ). The ocular fundus was normal and the cup-to disc ratio in each eye was about 0.3 (Fig. 1g). The umbilicus was normal (Fig. 1h). No heart defects, pituitary abnormalities, kidney abnormalities, neurological and skeletal anomalies were observed. This affected individual did not have obvious delayed gross motor development. The proband was diagnosed with ARS based on the ocular and systemic signs.

Genotyping
The average depth of the sequencing data was 103.24, the average coverage for data was 99.91%, the fraction of target regions covered with at least 10 × and 20 × was 98.96% and 96.76%, respectively. Variants remaining after filtering were manually assessed based on frequency / presence in known SNP databases, any Hearing  presented with posterior embryotoxon and evidence of iris adhesions. However, no dental defects, craniofacial dysmorphism and hearing loss were described in these two patients [18]. FOXC1 heterozygous variant c.516_518delGCG (p.Arg173del) was only found in the patient II:1 and was absent in his unaffected parents (Fig. 1b), consistent with autosomal dominant inheritance (de novo). Pathogenic computational verdict based on 1 pathogenic prediction from phyloP vs no benign prediction. According to the American College of Medical Genetics and Genomics (ACMG), c.516_518delGCG (p.Arg173del) is classified as a pathogenic variant (PS2 + PM1 + PM2 + PP3 + PP4) [16,17,19]. Two variants in ERCC6, c.2444G > A (p.Gly815Asp) and c.2125G > A (p.Val709Ile) were both classified as variants with uncertain significance. ERCC6 encodes a DNA-binding protein that is important in transcription-coupled excision repair. Pathogenic variants in ERCC6 are associated with Cockayne Syndrome, which is an autosomal recessive disorder and characterized by postnatal developmental failure, progressive  neurodegeneration, microcephaly, and premature aging. These phenotypes were not in accordance with the proband's clinical presentations. These data, together with the clinical presentation of the patient and consistent autosomal dominant inheritance of the FOXC1 gene, indicate that FOXC1 heterozygous variant c.516_518delGCG (p.Arg173del) is the cause of ARS in the proband.

Discussion
The FOXC1 gene (MIM #601090) encodes a transcription factor, FOXC1, which is characterized by a highly conserved approximately 110-amino-acid motif (69-178aa) known as the forkhead domain. The nuclear localization signals at either end of the forkhead domain support the transfer of FOXC1 to the nucleus and biding to DNA, thereby regulating the downstream target genes. FOXC1 is highly expressed in the heart, kidney and skeletal muscles, and has a role in tumor development, tissue-specific gene expression and embryogenesis. According to HGMD, 181 different pathogenic variants of FOXC1 have been identified, which are related with ARS and/or ASD (Anterior segment dysgenesis) (Additional file 1: Table 1, Fig. 2). Most pathogenic variants affect the amino acid within the forkhead domain, which impair the FOXC1 protein function by altering the ability of nuclear localization, transactivation activity, DNA-biding ability and protein stability [20,21]. Pathogenic variants at the C-terminal of FOXC1 are less characterized, probably influences FOXC1 protein ubiquitination [13].
Based on genetic analyses combined with ocular and the systemic abnormalities including craniofacial dysmorphism and dental malformation, we made a diagnosis of ARS in the proband [1]. Structure of the anterior segment was affected which is characterized by pupil deformity in both eyes. Apart from pupil deformity (corectopia), patients with ARS may have various anterior segment abnormalities such as posterior embryotoxon, iris stromal hypoplasia, pseudopolycoria and angle closure [22,23]. Among them, destruction of the chamber angle often leads to secondary glaucoma. Patients may develop into glaucoma at a very young age, or they may be asymptomatic for a long time from childhood to youth until high intraocular pressure occurs. It is reported that more than 50% patients with FOXC1-related ARS will develop into glaucoma eventually and the median onset age of glaucoma diagnosis is 6 ± 13.0 years [3,24,25]. In this study, although the 5-year-old boy had normal intraocular pressure and there were no alterations of the optic nerve, he is still at high risk of developing glaucoma. Due to the high risk and adverse consequence, it is crucial for the patients with ARS to follow up frequently and take a comprehensive ophthalmic examination. IOP monitoring, anterior chamber angle examination and fundus examination are necessary for follow-up. Automated perimetry and optic nerve head optical coherence tomography should be further improved to evaluate visual field defect and optic nerve injury in patients who are suspected to suffer from glaucoma. Early diagnosis and treatment are crucial to control the ocular complications of ARS and reduce the incidence of blindness caused by glaucoma. At present, surgical treatment is applied to decrease the raised IOP which correlates well with glaucoma progression and leads to satisfactory visual outcome in a long term [26].
Hearing loss is an infrequently characterized feature in ARS patients, with sensorineural hearing loss being the most prevalent type [27]. However, conductive hearing loss have been reported in several literatures (Table 1). Also, structural abnormalities of the cochlea have been observed in a few individuals. Although a precise mechanism for FOXC1 in hearing or ear development is not well understood. By systematic review of hearing phenotypes associated with FOXC1 pathogenic variants, 38 variants were reported to be related with abnormal hearing (Table 1), including 11 variants caused either a frameshift or premature stop codon and 17 gross deletions/insertions/complex rearrangements, leading to the total or partial loss of the FOXC1 function. Only one frameshift variant within the forkhead domain (p.Gln106Argfs*7) and 3 gross deletions reported normal hearing (Table 1) [28]. There are, however, many patients with FOXC1 variant involving the forkhead domain that do not report hearing problems. This observation may be due to variable expressivity of the hearing phenotype, or could implicate a second gene or other factors that impact hearing pathogenesis. Moreover, in many patients, there is no mention of the hearing phenotype, making it difficult to determine whether or not hearing tests were conducted. Although the proband in our study presented hearing loss, however, by detailed hearing evaluation, the diagnosis of conductive hearing loss induced by otitis media with effusion was reached. Hearing recovery and normal hearing was observed 3 months later, indicating that the hearing loss is reversible and coincidental and it might not linke to the FOXC1 variant.
Minor facial dysmorphism has been identified as part of the ARS spectrum since the initial reports of affected individuals, with characteristic facial features including maxillary hypoplasia with flattening of the midface, hypertelorism, a broad flat nasal root, and a thin upper lip [29]. Hypertelorism is typically a manifestation of a craniofacial deformity and not a disease in itself. It can be seen in a variety of conditions such as craniofacial cleft, craniofacial dysplasia and craniosynostosis syndromes, like Edwards Syndrome, 1q21.1 Duplication Syndrome, Basal Cell Nevus Syndrome, DiGeorge Syndrome Loeys-Dietz Syndrome, Apert Syndrome, Noonan syndrome, Neurofibromatosis, Leopard Syndrome, Crouzon Syndrome, Wolf-Hirschhorn Syndrome, Andersen-Tawil Syndrome, Waardenburg Syndrome and Cri-du-Chat Syndrome, et al. [30]. Assessment of dysmorphic features, including facial dysmorphism, plays a major role in the evaluation of genetic syndromes to reach a clinical diagnosis.
In summary, the present study described the clinical and genetic characteristics of a young Chinese boy with atypical ARS caused by a novel pathogenic variant in FOXC1, c.516_518delGCG (p.Arg173del), who was successfully diagnosed by whole exome sequencing (WES). This 3-bp deletion caused one Arginine loss, in the forkhead domain, might disrupt the secondary structure of the FOXC1 protein. Generally, children with FOXC1 variants are prone to developing into glaucoma and other ocular disorder, which underline the necessity of definite diagnosis by genetic methods along with subsequent early prevention of ocular defects. Regular monitoring concerning potential complications is required in ARS patients. The present results broadened the spectrum of FOXC1 variants in patients with ARS, especially within patients with atypical ARS.
Additional file 1. Summary of clinical features and molecular results in patients with FOXC1 pathogenic variants reported in HGMD and this study.