Retinitis pigmentosa and sensorineural deafness associated with a de novo DHX16 mutation: case report

Background: Retinitis pigmentosa and sensorineural deafness are two distinct clinical entities that can be caused by a variety of genetic mutations. The DHX16 gene, which encodes a protein involved in RNA processing, has been implicated in several genetic disorders. Here, we report a unique case of de novo DHX16 gene mutation presenting with both retinitis pigmentosa and sensorineural deafness.

Case Presentation: We describe the story of two 2-year-old girls who presented with progressive vision loss and hearing impairment. Both of these cases presented with de novo heterozygous mutations in the DHX16 gene. The mutation sites were NM_003587 c.2474C>T and NM_003587.5 c.1360C>T. Ophthalmological examination disclosed the classic stigmata of retinitis pigmentosa, while audiologic assessment revealed bilateral sensorineural hearing loss. Genetic testing identified a de novo mutation in the DHX16 gene, which was not present in the patients’ family histories. The patients were managed with supportive care, including hearing aids to improve their quality of life.

Conclusion: These cases highlight the importance of genetic testing in patients with combined retinitis pigmentosa and sensorineural deafness. Early identification of the underlying genetic mutation can facilitate appropriate management and genetic counseling for affected individuals and their families. Further research is needed to explore the pathophysiological mechanisms and potential therapeutic targets for DHX16-related disorders.

Background

Retinitis pigmentosa (RP) is a group of inherited retinal degenerative diseases characterized by progressive photoreceptor and retinal pigment epithelium degeneration, leading to significant vision loss (Bhatti, 2006; Suleman, 2025). Sensorineural deafness is a type of hearing loss that occurs due to damage to the inner ear, auditory nerve, or central auditory pathways (Saeed et al., 2025). Both conditions can be caused by mutations in various genes, and their co-occurrence can complicate diagnosis and management.

The DHX16 gene encodes a protein involved in RNA processing and has been associated with several genetic disorders (Drackley et al., 2024). Mutations in this gene can lead to a range of phenotypes, including developmental delay, neuromuscular disease, seizures, ocular nerve and/or retinal degeneration, and sensorineural hearing loss (SNHL) (Paine et al., 2019). Here, we present two cases of de novo DHX16 gene mutation resulting in both RP and sensorineural deafness. Usher syndrome represents the most typical condition characterized by the co-occurrence of RP and SNHL, inherited in an autosomal recessive manner. Based on the severity of hearing impairment and vestibular dysfunction, it is classified into three subtypes (USH1–3), among which USH1 and USH2 are the most prevalent (Delmaghani and El-Amraoui, 2022).

Additionally, Alport syndrome—caused by mutations in the COL4A3/4/5 genes—may occasionally present with both RP and SNHL, though renal abnormalities remain its predominant feature (Kashtan et al., 2018). Wolfram syndrome (DIDMOAD), resulting from WFS1 mutations, typically manifests with diabetes mellitus, optic atrophy, and SNHL, with some cases exhibiting RP-like retinal degeneration (Barrett et al., 1995). Mitochondrial disorders, such as maternally inherited diabetes and deafness (MIDD), may also demonstrate RP-like fundus changes in conjunction with SNHL (Murphy et al., 2008). Regarding the DHX16 gene, there is currently no definitive literature reporting its direct association with the co-occurrence of RP and SNHL.

Case presentation

Case 1, a 2-year-old female infant, presented with a complex medical history. Hearing screening performed 3 days after birth revealed failure in one ear. At 1 month of age, the well-child assessment documented absent visual tracking and auditory response. At 3 months of age, follow-up testing indicated bilateral hearing impairment. By 3 months, she also exhibited unstable head control and hypotonia (low muscle tone). Promptly following the hearing diagnosis at 5 months, genetic testing and electromyography (EMG) were initiated due to suspected genetic etiology. Genetic testing identified a de novo heterozygous mutation in the DHX16 gene: NM_003587 c.2474C>T (p. Ser825Phe) (Figure 1A).

Figure 1

Figure 1. Clinical features of case 1 with Retinitis pigmentosa and sensorineural hearing loss. (A) Sanger sequencing results of the genotypes of parents and child. (B) Sound pressure level testing used to assess the patient’s hearing level. (C) The results of the fundus examination of both eyes. (D) The results of the optical coherence tomography (OCT) examination of the patient.

Subsequent diagnostic audiological evaluation at 5 months of age confirmed a diagnosis of severe sensorineural hearing loss. Developmental concerns were noted early. Prior to cochlear implantation (CI) at 8 months of age, pre-and post-aided audiometric thresholds were documented as follows: Right ear (unaided): No response across 125–6,000 Hz at 90–120 dB HL. Right ear (aided): Responses observed at 250–2000 Hz with thresholds of 75–95 dB HL. Left ear (unaided): No response across 125–6,000 Hz at 90–120 dB HL. Left ear (aided): Responses detected at 250–500 Hz with thresholds of 75–95 dB HL (Figure 1B).

Ophthalmic evaluation at 1 month of age revealed bilateral lens opacities. By 14 months of age (1 year and 2 months), an ophthalmic examination detected no light perception (NLP), leading to a subsequent diagnosis of Leber congenital amaurosis (LCA). The examination demonstrated findings diagnostic of retinitis pigmentosa, featuring waxy pallor of the optic disks, attenuation of retinal vessels, grayish retinal discoloration, and pigmentary mottling (Figure 1C), with bilateral loss of foveal reflex obscuring anatomical localization of the central fovea (Figure 1D).

Case 2, a 2-year-old female infant, presented with a history of failed newborn hearing screening, absent visual tracking, and global developmental delay. Ophthalmologic examination revealed fundus abnormalities. Follow-up audiological assessment at 3 months of age confirmed persistent bilateral hearing impairment. By 7 months of age, a comprehensive diagnostic evaluation established definitive diagnoses of severe sensorineural hearing loss, bilateral retinal degeneration, and macular atrophy. Enrollment in a rare disease research program at 8 months of age included genetic analysis, which identified a de novo heterozygous mutation in the DHX16 gene: NM_003587.5 c.1360C>T (p. Arg454Trp) (Figure 2A). She was ultimately diagnosed with LCA and sensorineural hearing loss.

Figure 2

Figure 2. Clinical features of case 2 with Retinitis pigmentosa and sensorineural hearing loss. (A) Sanger sequencing results of the genotypes of parents and child. (B) The auditory Steady-State Response test of the patient. (C) The results of the fundus examination of both eyes.

Auditory steady-state response (ASSR) testing was performed using Eclipse 10 stimuli at modulation rates of 77–100 Hz. Results demonstrated that right ear absence of reproducible responses across 500–4,000 Hz at maximum stimulus intensity of 100 dB nHL. The left ear shows no detectable responses at 500–2000 Hz at 100 dB nHL, but a significant response was present at 4,000 Hz (threshold: 95 dB nHL) (Figure 2B).

At 8 months of age, the infant underwent fundus screening, which revealed retinitis pigmentosa in both eyes with macular lesions. Upon follow-up examination at 2.5 years of age, fundus examination showed diffuse bone-spicule pigmentation in both retinas, involving the macular area. The macula exhibited a yellowish discoloration with pigmentary disturbances (Figure 2C).

The patient was managed with supportive care to improve quality of life. Low-vision aids were provided to assist with daily activities, and hearing aids were fitted to address the hearing impairment. Regular follow-up appointments were scheduled to monitor the progression of the disease and provide ongoing support. Clinical and genetic characteristics of patients with DHX16 variants are listed in Table 1, and key events and metrics are listed in Table 2.

Table 1

Table 1. Clinical and genetic characteristics of patients with DHX16 variants.

Table 2

Table 2. Timeline of patient care: key events and metrics.

ClustalX-based alignment revealed that the amino acid substitution site (Ser825) is evolutionarily conserved across multiple species, including human, chimpanzee, mouse, horse, alpaca, chicken, anole lizard, and Caenorhabditis elegans (Figure 3A). In silico analysis of the DHX16 variant c.2474C>T (p. Ser825Phe) further confirmed the high conservation of the Ser825 residue.

Figure 3

Figure 3. Molecular characterization of pathogenic DHX16 variants: evolutionary conservation analysis and clinical spectrum. (A) ClustalX alignment demonstrates evolutionary conservation of the pathogenic DHX16 Ser825Phe variant across eight species. (B) ClustalX alignment reveals evolutionary conservation of the Arg454 residue across eight vertebrate and invertebrate species. (C) Systematic review identifies 18 pathogenic DHX16 variants (89% missense) in human cases.

Multiple sequence alignment using ClustalX demonstrated that the amino acid substitution site (Arg454) is evolutionarily conserved across diverse species, including human (Homo sapiens), chimpanzee (Pan troglodytes), mouse (Mus musculus), horse (Equus caballus), alpaca (Vicugna pacos), chicken (Gallus gallus), anole lizard (Anolis carolinensis), and nematode (Caenorhabditis elegans) (Figure 3B). In silico analysis of the DHX16 missense variant c.1360C>T (p. Arg454Trp) further confirmed the high degree of conservation at this residue position.

We systematically reviewed all published DHX16 variants in human cases, identifying a total of 18 distinct DHX16 variants (including those reported in the present study). Among these, missense variants predominated (n = 16, 89%), while small deletions accounted for the remaining cases (n = 2, 11%) (Figure 3C). When we checked the frequency of the identified variants in population databases, we found that the variants c.2474C>T and c.1360C>T were absent from major population databases such as 1,000 Genomes (2015aug_all) and ESP6500SI. Based on the ACMG/AMP guidelines, the variant c.2474C>T is classified as likely pathogenic, supported by its confirmed de novo origin with absence in both parents, its absence from control populations, and the high concordance between the patient’s specific clinical presentation and a disease with a monogenic etiology associated with this gene. The variant c.1360C>T is classified as pathogenic according to the ACMG/AMP guidelines. This definitive classification is supported by multiple lines of evidence: its established presence in literature databases as a known disease-causing variant, the confirmation of its de novo origin through parental segregation studies, its absence in control populations, and the high specificity of the patient’s phenotype to a monogenic disorder associated with this gene. We also checked the pathogenicity of the identified variant on different online software (Table 3).

Table 3

Table 3. Pathogenicity of the variant c.2474C>T on different online software.

Discussion and conclusion

This case highlights the importance of genetic testing in patients presenting with combined retinitis pigmentosa and sensorineural deafness. The identification of a de novo mutation in the DHX16 gene underscores the genetic heterogeneity of these conditions and the potential for novel mutations to cause complex phenotypes. Our patients exhibited significant neurological features beyond the core phenotypes of RP and SNHL, which have not been emphasized in previous reports linking DHX16 to isolated sensory impairments. Specifically, both patients presented with global developmental delay, including hypotonia (Case 1) and delayed motor development (Case 2). These findings are crucial as they suggest that DHX16-related disorders may encompass a broader neurodevelopmental spectrum, rather than being confined to purely sensory deficits. This expands the clinical profile associated with DHX16 mutations and distinguishes our cases from the classic presentation of syndromes like Usher syndrome, where such pronounced global developmental delay is not a hallmark feature. The concomitant presentation of RP and SNHL is a hallmark of Usher syndrome (USH). This genetically heterogeneous condition is classified into three types: the most severe form, USH1, caused by mutations in genes that include MYO7A and CDH23 (Nakanishi et al., 2010). The most prevalent form, USH2, primarily results from defects in USH2A (Zhu et al., 2021). USH3 is characterized by variable progression and is mainly associated with mutations in the CLRN1 gene (Wang et al., 2024).

The DHX16 gene is involved in RNA processing, and its mutations can lead to a variety of clinical manifestations (Drackley et al., 2024). The co-occurrence of retinitis pigmentosa and sensorineural deafness in these two patients suggests a possible role of the DHX16 gene in both retinal and auditory function. We have prepared a mutation table for the DHX16 report and mentioned the zygosity of the variations as well as the reported phenotypes for each variation (Table 4).

Table 4

Table 4. Mutations of DHX16 and reported phenotypes for each variant.

Mutations in pre-mRNA splicing factors represent the second-most common cause of autosomal dominant retinitis pigmentosa (adRP) and constitute a major source of vision loss (Hafler et al., 2016). For instance, pathogenic variants in the pre-messenger RNA (pre-mRNA) splicing factor 31 (PRPF31) gene cause autosomal dominant retinitis pigmentosa. The key genes that have been identified so far include PRPF31, PRPF3, PRPF4, PRPF6, PRPF8, and SNRNP200, which encode the core components of the spliceosome. DHX16 may be functionally analogous in this context (Stephenson et al., 2025).

Retinal photoreceptors and cochlear hair cells exhibit a shared vulnerability to degeneration, primarily attributed to their intrinsically high metabolic demands and heightened sensitivity to apoptotic pathway activation (Liu et al., 2007). Mutations in DHX16 disrupt pre-mRNA splicing fidelity, resulting in aberrant transcripts for key genes essential for retinal photoreceptor and cochlear hair cell function, including those involved in phototransduction and hair cell ciliary structure/function.

In vitro studies demonstrate that mutant DHX16 impairs spliceosome function, resulting in the nuclear accumulation of unspliced pre-mRNA from multiple intron-containing genes. This defect stems from the mutant protein’s formation of a catalytically inactive spliceosomal complex through its interaction with the G-patch protein GPKOW, exerting a dominant-negative effect (Bohnsack et al., 2021; Gencheva et al., 2010). The nuclear accumulation of aberrant transcripts exerts detrimental effects on cellular function through both the toxicity of their high abundance and the concurrent reduction in functional protein expression, as unspliced mRNAs retained within the nucleus are unavailable for translation. Pathogenic variants in other DExD/H-box RNA helicase superfamily members cause comparable phenotypes, often characterized by aberrant central nervous system (CNS) development, which may or may not include extra-CNS anomalies (Paine, Posey, Grochowski, Jhangiani, Rosenheck, Kleyner, Marmorale, Yoon, Wang, Robison, Cappuccio, Pinelli, Magli, Akdemir, et al., 2019; Blok et al., 2015). Future diagnostic screening panels for retinitis pigmentosa with concurrent hearing loss should consider including DHX16. Targeted therapeutic interventions for DHX16-related pathology remain an unmet clinical need.

Retinitis pigmentosa and other degenerative eye diseases have long been considered “irreversible” blinding disorders, characterized by symptoms such as night blindness and progressive visual field constriction, often leading to gradual vision loss and impaired quality of life. While traditional approaches such as gene therapy, optogenetics, or earlier-generation stem cell treatments have demonstrated limited efficacy, they remain constrained by significant technical challenges. Currently, multiple therapeutic strategies are being explored for patients with RP. Notably, the latest breakthrough involving human ciliary margin-derived retinal stem cells (hNRSCs) has achieved precise localization, functional validation, and retinal repair in animal models for the first time, offering end-stage patients a transformative potential—from “disease delay” to “tissue regeneration” (Liu et al., 2025).

Currently, clinical interventions for SNHL include hearing aids, vasodilators, neurotrophic drug therapy, and cochlear implants. However, these approaches cannot fully restore hearing but only provide partial improvement, with their efficacy remaining limited—particularly for patients with profound deafness (Kelleci and Golebetmaz, 2023). In recent years, alongside advancements in biotechnology, stem cell therapy has emerged as a prominent research focus in otology. Upon damage to the normal ear structure, stem cells can leverage their multipotent differentiation potential to regenerate functionally and morphologically equivalent tissues, migrating to the injured cochlear regions to facilitate repair (Bergman et al., 2021). This mechanism precisely addresses the inherent irreplaceability of inner ear hair cells, offering a promising therapeutic strategy (Mohammadian et al., 2017; Chorath et al., 2020). Currently, inducing functional hair cells via inner ear stem cell differentiation to replace damaged hair cells is considered to be a feasible treatment for sensorineural hearing loss (Qi et al., 2024).

Further research is needed to elucidate the pathophysiological mechanisms underlying DHX16-related disorders and to identify potential therapeutic targets.

In conclusion, this case report emphasizes the significance of genetic testing in diagnosing and managing patients with combined retinitis pigmentosa and sensorineural deafness. Early identification of the underlying genetic mutation can facilitate appropriate management strategies and genetic counseling for affected individuals and their families. Continued research into the role of the DHX16 gene in retinal and auditory function is essential for advancing our understanding and treatment of these disorders. The identification of de novo DHX16 mutations in these patients with concurrent LCA and SNHL carries significant implications for both clinical practice and research. These cases underscore the necessity of incorporating DHX16 into targeted genetic screening panels for neonates presenting with failed hearing screening or early-onset visual impairment, particularly when accompanied by developmental delay. The conserved nature of the mutated residues (Ser825 and Arg454) across species and their predicted impact on RNA splicing suggest a shared molecular mechanism underlying both retinal and cochlear pathology, possibly through disrupted processing of photoreceptor- and hair cell-specific transcripts. From a therapeutic standpoint, while current interventions such as cochlear implantation and low-vision aids provide symptomatic relief, emerging RNA-targeted approaches and stem cell therapies offer promising avenues for addressing the root cause of DHX16-related dysfunction. Early genetic diagnosis could substantially reduce healthcare costs by avoiding prolonged diagnostic odysseys while enabling timely intervention to preserve residual sensory function. Moving forward, concerted efforts should focus on establishing animal models to validate genotype–phenotype correlations, expanding multicenter studies to characterize variant-specific clinical manifestations, and conducting rigorous cost-benefit analyses of cascade genetic testing for at-risk family members. These cases highlight how rare genetic disorders can serve as models for understanding fundamental biological processes while simultaneously driving innovations in precision medicine for sensory impairments.

Data availability statement

The original contributions presented in the study are included in the article/supplementary material; further inquiries can be directed to the corresponding author.

Ethics statement

The studies involving humans were approved by the Ethics Committee of Jinan Maternal and Child Health Hospital. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation in this study was provided by the participants’ legal guardians/next of kin. Written informed consent was obtained from the minor(s)’ legal guardian/next of kin for the publication of any potentially identifiable images or data included in this article.

Author contributions

LW: Formal Analysis, Data curation, Validation, Methodology, Project administration, Investigation, Writing – original draft. JG: Investigation, Writing – original draft, Conceptualization, Formal Analysis, Project administration, Data curation, Validation. MS: Project administration, Writing – original draft, Data curation, Validation, Investigation. LF: Writing – original draft, Investigation, Data curation. SW: Writing – original draft, Data curation, Investigation. XL: Software, Writing – original draft, Data curation. SG: Investigation, Writing – original draft, Data curation. BH: Writing – review and editing, Funding acquisition, Resources, Visualization, Formal Analysis.

Funding

The author(s) declare that financial support was received for the research and/or publication of this article. This work was supported by the Project of the Health Commission of Jinan City, China (Project approval number: 2024307016).

Acknowledgements

The authors would like to thank all the family members for their participation and cooperation in this study. The authors also thank Yinggang Liu (Mygeno Beijing) for assistance in data collection.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Abbreviations

ASSR, Auditory steady-state response; CNS, Central nervous system; EMG, Electromyography; LCA, Leber congenital amaurosis; RP, Retinitis pigmentosa; SNHL, Sensorineural hearing loss.

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