# The Cortico-Cortical and Subcortical Circuits of the Human Brain Language Centers Including the Dual Limbic and Language Functioning Fiber Tracts

**Authors:** Arash Kamali, Nithya P. Narayana, Anastasia Loiko, Anusha Gandhi, Paul E. Schulz, Nitin Tandon, Manish N. Shah, Vinodh A. Kumar, Larry A. Kramer, Jay-Jiguang Zhu, Haris Sair, Roy F. Riascos, Khader M. Hasan

PMC · DOI: 10.3390/brainsci16020142 · Brain Sciences · 2026-01-28

## TL;DR

This review explores brain circuits involved in language and emotion, showing how they overlap and impact disorders like dyslexia and autism.

## Contribution

The paper introduces the Kamali limbic model, highlighting dual-function fiber tracts linking language and limbic systems.

## Key findings

- Advanced imaging reveals a more interconnected language network beyond the dual-stream model.
- Dual limbic-language pathways are linked to disorders with cognitive and emotional symptoms.
- The Kamali model identifies distinct ventral and dorsal limbic networks with overlapping functions.

## Abstract

Background/Objectives: In recent years, MRI-based diffusion-weighted tractography techniques have uncovered additional white matter pathways that have significant roles in language processing and production. In this review, we aim to outline the major language centers of the brain and major language pathways along with association tracts that serve dual roles in both the language and limbic systems. According to the current dual-stream model of language processing, the brain’s language network is organized into a dorsal stream, responsible for mapping sound to articulation, and a ventral stream, which maps sound to meaning. Materials and Methods: The literature cited in this manuscript was identified through targeted searches of the PubMed database. Priority was given to peer-reviewed human studies, including original neuroimaging, cadaveric validation, and intraoperative stimulation studies. Non-peer-reviewed sources and publications lacking clear anatomical or functional correlation to language pathways were excluded. Results: Advances in functional MRI and diffusion weighted imaging techniques have revealed a more interconnected network, expanding our understanding beyond the classical dual-stream model of language processing. The Kamali limbic model proposed distinct ventral and dorsal limbic networks. Notably, several fiber pathways within the ventral limbic network may subserve both language and limbic functions. The association tracts with dual limbic-language functions form a critical basis for understanding the pathophysiology of language disorders accompanied by cognitive and emotional comorbidities observed in dyslexia, speech apraxia, aphasia, autism spectrum disorder, schizophrenia and post-traumatic stress disorder. Conclusions: Visualizing the language center and interconnected dual language and limbic fiber tracts highlights the importance of integrating language, executive function, and emotion in developing disease models and designing effective, targeted treatments for patients.

## Linked entities

- **Diseases:** dyslexia (MONDO:0005489), aphasia (MONDO:0000598), autism spectrum disorder (MONDO:0005258), schizophrenia (MONDO:0005090), post-traumatic stress disorder (MONDO:0005146)

## Full-text entities

- **Genes:** SGPL1 (sphingosine-1-phosphate lyase 1) [NCBI Gene 8879] {aka NPHS14, RENI, S1PL, SPL}, FAT1 (FAT atypical cadherin 1) [NCBI Gene 2195] {aka CDHF7, CDHR8, FAT, ME5, hFat1}, FOXK2 (forkhead box K2) [NCBI Gene 3607] {aka ILF, ILF-1, ILF1, nGTBP}, SMN1 (survival of motor neuron 1, telomeric) [NCBI Gene 6606] {aka BCD541, GEMIN1, SMA, SMA1, SMA2, SMA3}, ATR (ATR checkpoint kinase) [NCBI Gene 545] {aka FCTCS, FRP1, MEC1, SCKL, SCKL1}, MAPT (microtubule associated protein tau) [NCBI Gene 4137] {aka DDPAC, FTD1, FTDP-17, MAPTL, MSTD, MTBT1}
- **Diseases:** aphasic syndromes (MESH:D013577), Broca's aphasia (MESH:D001039), Parkinson's disease (MESH:D010300), Foix-Chavany-Marie syndrome (MESH:C537069), akinetic mutism (MESH:D000405), Damage to the SMA (MESH:D017034), ASD (MESH:D000067877), Fronto-Occipital Fasciculus (MESH:D006259), Fasciculus III (MESH:C537189), optic ataxia (MESH:D001259), primary progressive aphasia (MESH:D018888), epilepsy (MESH:D004827), gliomas (MESH:D005910), Wernicke's aphasia (MESH:D001041), AF (MESH:D012607), thalamic aphasia (MESH:D013786), Damage to the DLPFC (MESH:D014854), Developmental dyslexia (MESH:D004410), injury to (MESH:D014947), schizophrenia (MESH:D012559), anxiety (MESH:D001007), Damage to the IFOF (MESH:D056989), Wernicke's area (MESH:D014899), aphasia (MESH:D001037), developmental language disorders (MESH:D007805), traumatic brain injury (MESH:D000070642), hemiparesis (MESH:D010291), impaired syntax (MESH:D060825), psychiatric disorders (MESH:D001523), conduction aphasia (MESH:D018886), dementia (MESH:D003704), aggression (MESH:D010554), stroke (MESH:D020521), CB (MESH:D058606), bipolar disorder (MESH:D001714), palsy (MESH:D010243), dysarthria (MESH:D004401), agnosia (MESH:D000377), OCD (MESH:D009771), depression (MESH:D003866), Cerebellar infarcts (MESH:D007238), white matter abnormalities (MESH:D056784), impaired language comprehension (MESH:D007806), deficits in speech production (MESH:D013064), articulatory disorders (MESH:D001072), prosopagnosia (MESH:D020238), dysfunctions of spatial awareness (MESH:D008569), brain tumor (MESH:D001932), psychiatric communication deficits (MESH:D003147), Longitudinal Fasciculus II (MESH:D017887), Damage (MESH:D020263), behavioral or cognitive impairment (MESH:D003072), PTSD (MESH:D013313), cerebellar cognitive affective syndrome (MESH:D002526), multiple sclerosis (MESH:D009103), semantic (MESH:D057180), Major Depressive Disorder (MESH:D003865), Emotional dysregulation (MESH:D021081)
- **Chemicals:** EmC (-), water (MESH:D014867)
- **Species:** Macaca mulatta (rhesus macaque, species) [taxon 9544], Cercopithecidae (monkey, family) [taxon 9527], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938411/full.md

## References

170 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938411/full.md

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Source: https://tomesphere.com/paper/PMC12938411