Autism & ADHD:
Supporting Every Child’s Potential
Understanding Autism & ADHD‍
Non-invasive Cytotron RFQMR-FRB therapy targeting neural connectivity, attention regulation, and sensory processing in Autism Spectrum Disorder and ADHD. CDSCO approved. Bengaluru.
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Autism Spectrum Disorder (ASD): ASD is characterised by differences in social communication and interaction, restricted and repetitive patterns of behaviour, and variable sensory processing. Underlying these presentations is a pattern ofatypical neural connectivity: local over-connectivity within specific brain regions and long-range under connectivity between regions — particularly the prefrontal cortex, temporal lobes, and the default mode network. GABAergic inhibition is dysregulated,contributing to sensory hypersensitivity and cortical excitability. There is no cure for ASD. The goal of therapy is functional improvement — supporting the brain’s own capacity to build more effective connections.

Attention Deficit Hyperactivity Disorder (ADHD):  ADHD is characterised by persistent inattention, hyperactivity, and impulsivity that impair functioning across settings. The neuro biological basis is primarily a dysfunction in prefrontal-subcortical circuits governing executive function — specifically deficits in dopaminergic and noradrenergic neuro transmission that impair working memory, sustained attention, response inhibition, and planning. Structural and functional imaging consistently shows reduced activation and connectivity in the prefrontal cortex and itsconnections to the basal ganglia and cerebellum during attentional tasks. ADHD is typically managed with stimulant medication and behavioural interventions; Cytotron is positioned as a complementary modality.‍
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Improving social engagement, communication, and eye contact
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Supporting sustained attention, focus, and impulse regulation
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Reducing sensory hypersensitivity and emotional dysregulation
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Complementing ABA, speech therapy, occupational therapy, and medication
Understanding
Autism and ADHD
Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) are both neuro developmental conditions rooted in differences in brain connectivity, neuro transmitter signalling, and cortical organisation. While they are distinct diagnoses, they frequently co-occur — an estimated 30–80% of individuals with autism also meet diagnostic criteria for ADHD — and they share overlapping biophysical signatures that RFQMR-FRB therapy can address.
PRECISION ADMISSION
BEFORE TREATMENT BEGINS
Clinical Review Assessment Table
Assessment Area What is Reviewed
Medical/Injury History Diagnosis history, prior neurological events, birth and developmental history, co-occurring conditions, current medications
Neuroimaging MRI of the brain is required for dosimetry planning. The treating team reviews existing imaging and may request updated scans before confirming treatment
Implants/Devices Any metallic implants, cochlear implants, cardiac devices, VP shunts, or other implanted hardware. Presence of an implant does not automatically exclude treatment but must be disclosed and formally assessed by the clinical team
Active Conditions Active infections, uncontrolled seizure disorders requiring acute management, recent surgical procedures, or other conditions that may affect treatment timing or safety
Current Treatment Ongoing ABA, speech, occupational, or pharmacological management — to confirm Cytotron is integrated appropriately and no conflicts exist with current protocols
How RFQMR-FRB Therapy Helps?
In both ASD and ADHD, the central neuro biological challenge is not structural destruction of neurons — as instroke or HIE — but rather suboptimal connectivity, dysregulated neuro transmission, and an atypical biophysical environment that limits the brain’s ability to form and strengthen the circuits it needs. RFQMR-FRB therapy actson the underlying cellular and molecular environment to support the brain’s own capacity for reorganisation and functional improvement.

The therapy delivers precisely calibrated rotating electromagnetic pulses in the non-ionising spectrum. These pulses modulate transmembrane potential, activate endogenous neurotrophic and synaptic plasticity pathways, and support the biophysical conditions necessary for improved neural communication.
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BDNF Upregulation — Synaptic Density and Connectivity
Brain-Derived Neurotrophic Factor (BDNF) is a critical regulator of synaptic strength, dendritic branching, and neural circuit formation. BDNF levels are consistently found to be reduced in individuals with ASD and ADHD. RFQMR stimulation up regulates BDNF expression, promoting the growth and strengthening of synaptic connections. In the context of autism, increased BDNF activity supports the long-range connectivity deficits that underlie social and communicative processing. In ADHD, it supports thestrengthening of prefrontal circuits involved in sustained attention and working memory.
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Ca² -Calmodulin-CREB Pathway — Synaptic Plasticity
RFQMR promotes controlled, therapeutic calcium influx through voltage-gated channels. Intra cellular calcium activates calmodulin, which phosphorylates CREB (cAMP Response Element - Binding  protein). Activated CREB drives gene transcription essential for synaptic plasticity, long-term potentiation, and theformation of new neural pathways. This pathway is fundamental to the brain’s capacity to reorganise its circuitry in response to experience — a process that is impaired in both ASD and ADHD. CREB activation supports the consolidation of new behavioural and cognitive patterns acquired through concurrent therapy.
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Transmembrane Potential (TMP) Normalisation — Cortical Regulation
Neurons in the autistic and ADHD brain exhibit a typical transmembrane potential patterns, contributing to dysregulated cortical excitability — a state associated with sensory hypersensitivity, motional dys regulation, and the reduced signal-to-noise ratio in attentional networks. RFQMR-FRB directly modulates TMP across target neural tissue, working toward a more balanced electro chemical environment. This contributes to reduced cortical hyper excitability, improved sensory gating, and a calmerbaseline state from which behavioural and cognitive improvement can proceed.
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MAPK/ERK Cascade — Neural Progenitor and Glial Support
The MAPK/ERK signalling cascade, stimulated by RFQMR-induced biophysical modulation, promotes the activity of neural progenitor cells and supports glial cell function. In neuro developmental contexts, glialcells — particularly astrocytes and oligodendrocytes — play critical roles in synapse formation, myelination of developing circuits, and the metabolic support of active neurons. Supporting glial health and progenitor activity contributes to the broader cellular environment in which improved connectivity can develop.
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Dopaminergic and GABAergic Circuit Support
ADHD is fundamentally a disorder of dopaminergic and noradrenergic prefrontal signalling. ASD involves dysregulated GABAergic inhibitory tone, contributing to sensory hypersensitivity and social communication difficulties. RFQMR’s modulation of TMP and activation of neurotrophic factors — particularly BDNF andGDNF — supports the health and signalling efficiency of these neuro transmitter systems. GDNF, upregulated during RFQMR therapy, provides trophic support for dopaminergic neurons. Improved GABAergic tone, supported by TMP normalisation, contributes to calmer sensory processing and reduced cortical over activation.
What Improvement Looks Like
Social Communication and Engagement
In children with ASD, families have reported improvements in eye contact, responsiveness to their name, turntaking in interaction, and the initiation of social contact. Verbal children may show expanded vocabulary and more spontaneous communication. Non-verbal or minimally verbal children may show increased use of alternative communication systems and greater engagement with their environment. These gains reflect improved functional connectivity between the temporal, frontal, and limbic regions involved in social processing.
Attention, Focus, and Impulse Regulation
In children with ADHD, and in the ADHD presentations that co-occur with ASD, families and educators haveobserved improvements in the ability to sustain attention on tasks, reduced impulsivity in social and academic settings, and improved working memory. These gains are consistent with improved prefrontal-subcortical circuit function. Cytotron is used as a complementary modality and does not replace existing pharmacological or behavioural management.
Sensory Processing and Emotional Regulation
Sensory hypersensitivity — to sound, light, texture, or touch — is a significant source of distress in ASD andcontributes to emotional dysregulation and melt down behaviours. TMP normalisation and improved GABAergic tone may contribute to a calmer sensory baseline, reduced sensory-triggered distress, and improved emotional self-regulation over the course of treatment and follow-up.
Developmental Milestone Acquisition
In younger children with ASD and co-occurring developmental delay, families have reported acceleration in developmental milestone acquisition — including play skills, motor imitation, self-care, and early academicreadiness. These gains are most pronounced when Cytotron is combined with structured therapeutic intervention(ABA, speech, occupational therapy) during and after the treatment cycle. For developmental gains of this nature,the full picture typically emerges after three cycles: early cycles may produce subtle shifts in engagement andresponsiveness, with more pronounced functional gains consolidating through the second and third cycles. Individual response varies and cannot be predicted in advance.
Neural Connectivity
BDNF-driven synaptic strengthening and long-rangecircuit support
Synaptic Plasticity
CREB-mediated pathway for new circuit formation
Cortical Regulation
TMP normalisation reducing sensoryhyperexcitability
Attention & Focus
Prefrontal dopaminergic circuit support for ADHD

Everything You Need
to Know—Upfront

We help patients and healthcare partners navigate personalized care and innovative medtech solutions—here’s what most people ask before getting started with us
Can Cytotron therapy help children with Autism?

Cytotron RFQMR-FRB therapy aims to support neural connectivity and synaptic function in children withAutism Spectrum Disorder. By activating BDNF, CREB-mediated plasticity, and TMP normalisation pathways, the therapy targets the underlying biophysical environment of the autistic brain. Improvement isfunctional and gradual — not a cure — but families have reported gains in social engagement,communication, eye contact, and sensory tolerance.

Can Cytotron therapy help children with ADHD?

In ADHD, RFQMR-FRB therapy targets the prefrontal cortical circuits involved in attention regulation,working memory, and impulse control. By modulating transmembrane potential and supportingdopaminergic and noradrenergic signalling pathways, therapy may improve sustained attention, reduceimpulsivity, and support executive function. Cytotron is used as a complementary modality along side existing behavioural and pharmacological management.

Is Cytotron treatment safe for children with ASD or ADHD?

Cytotron RFQMR-FRB therapy is non-surgical, painless, and does not involve radiation, injections, or anaesthesia. Each session lasts approximately 60 minutes and a parent or carer may remain present throughout. There are no known side effects at prescribed clinical dosimetry. Before treatment is confirmed, every child undergoes a structured clinical assessment by Ardram’s medical team covering medical history, neuroimaging, implants and devices, active conditions, and current therapies. This assessment screens for contraindications and ensures the treatment plan is appropriate for the individual child. Eligibility is not assumed — it is determined.

Can Cytotron be used alongside ABA, speech therapy, occupational therapy, ormedication?

Yes. Cytotron is routinely integrated with Applied Behaviour Analysis (ABA), speech and language therapy, occupational therapy, and pharmacological management including stimulant medication for ADHD. It doesnot require any existing treatment to be discontinued or modified. The regenerative effects of RFQMR-FRBmay enhance the brain’s responsiveness to concurrent behavioural and educational interventions.

My child has both Autism and ADHD. Can Cytotron address both?

Yes. The biophysical mechanisms targeted by RFQMR-FRB therapy — BDNF up regulation, CREBmediated synaptic plasticity, TMP normalisation, and dopaminergic circuit support — are relevant to bothconditions simultaneously. A significant proportion of children with ASD also meet criteria for ADHD. Thepersonalised dosimetry plan is designed to target the specific brain regions and connectivity patternsidentified in the individual child’s MRI and clinical profile

What age range is suitable for treatment?

Eligibility is assessed individually through Ardram’s structured clinical assessment process, which covers the child’s neuro imaging, developmental and medical history, current therapies, and a systematic review of contraindications. There is no single fixed lower age limit; suitability is determined by the clinical team for each individual. Contact us to discuss your child’s specific situation and we will advise on next steps.