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Case Report
ARTICLE IN PRESS
doi:
10.25259/ABMH_44_2025

Gratification Syndrome in a Young Girl: A Diagnostic Dilemma Mimicking Seizure Disorder – A Case Report

Department of Psychiatry, Gauhati Medical College and Hospital, Bhanagagarh, Guwahati, Assam, India.

*Corresponding author: Anupam Tamuli, Department of Psychiatry, Gauhati Medical College and Hospital, Bhanagagarh, Guwahati, Assam, India. aanupam555@gmail.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Medhi D, Tamuli A. Gratification Syndrome in a Young Girl: A Diagnostic Dilemma Mimicking Seizure Disorder – A Case Report. Acad Bull Ment Health. 2025; doi: 10.25259/ABMH_44_2025

Abstract

Gratification behavior or infantile masturbation is an underrecognized condition in young children that often mimics seizure-like episodes. A case of a young girl brought to the Psychiatry outpatient department of Gauhati Medical College with repetitive abnormal limb movements and behaviors of genital stimulation misinterpreted as seizures is presented here. Patients' symptoms were observed to subside with distraction and were not associated with typical symptoms of seizure, such as altered consciousness, incontinence, or post-ictal confusion. Past history of multiple episodes of seizure generalised tonic clonic seizure following head trauma and treatment with antiepileptics further complicated the clinical picture. Normal Electroencephalogram and absence of neurological findings, along with the disappearance of symptoms following distraction, led to the diagnosis of gratification syndrome. Appropriate psychoeducation, adjustment of the dose of antiepileptics, and therapeutic behavioral strategies led to significant symptom improvement. This case highlights the importance of differentiating gratification behavior from seizure disorders to avoid unnecessary investigations and stigmatization.

Keywords

Behavioral disorder
Gratification syndrome
Infantile masturbation
Seizure mimic

INTRODUCTION

Gratification syndrome, often termed as “infantile masturbation,” is a benign and self-limiting behavior observed in young children, often misdiagnosed due to its atypical and variable presentations.[1] Unlike adult masturbation, this behavior is usually non-genital in nature and may involve rhythmic body movements, posturing, or limb stiffening.[2] Due to a lack of awareness among clinicians and caregivers, it is frequently mistaken for seizure disorders, movement disorders, or even signs of abuse, leading to misdiagnosis, unnecessary investigations, and distress.[3] A diagnostically challenging case of gratification behavior in a female child presenting with abnormal jerky limb movements and perineal stimulation, initially suspected to be seizure disorder, is reported here.

CASE REPORT

A girl child aged 2 years 11 months was brought to the Psychiatry out patient department of Gauhati Medical College and Hospital by her parents with complaints of repeated abnormal jerky movements of both upper and lower limbs, primarily occurring while lying in the prone position. During these episodes, the child was observed to press clothes or nearby objects against her perineal region. A short video clip demonstrating the child’s typical gratification episode was recorded and shown in the Video 1. These events occurred 10–15 times a day, lasted variably in minutes, and were occasionally followed by sleep. Notably, the episodes were never observed during sleep and tended to increase when the child was left alone and subsided with distraction by parents with verbal stimuli or engagement in other activities. There was no history of frothing, incontinence, clenching of teeth, or loss of consciousness associated with these events. Due to the motor features and stereotyped nature of episodes, a seizure disorder was initially considered. The child had a history of head injury at around 1 year of age following a fall from a height of 2–3 feet. The girl started to have multiple episodes of abnormal jerky movements of all limbs with stiffening of the body, associated with frothing and transient unresponsiveness lasting for 1–2 minutes after a few days of falling till she was 2 years old. However, there was no associated tongue bite or incontinence. She was evaluated by a neurologist at that time; Magnetic resonance imaging brain, computed tomography scan, and electroencephalogram (EEG) were reported normal. By looking at her presenting symptoms, a provisional diagnosis of Generalised tonic clonic seizure was made. She was started on syrup Levetiracetam and over the next year, her episodes subsided, though Levetiracetam was advised to continue.She remained symptom-free for a few months. But, around the age of 2 years, the child developed a new set of behaviors described above. EEG repeated at this stage once again revealed a normal awake record. The episodes were now distinct from the past seizures involving perineal stimulation and stereotyped positioning, without any impairment of consciousness. She was born to non-consanguineous parents, delivered via lower segment cesarean section due to premature rupture of membranes, with a birth weight of 2.3 kg. There were no NICU admissions or perinatal complications. Milestones were appropriate for age, except for a mild delay in speech, for which she was undergoing speech therapy. No signs of pain, abdomen or urinary tract infection were found on physical or laboratory evaluation.General and systemic examination revealed no findings. Neurological examination revealed no deficit. Mental status examination was within normal limits for age and development. A multidisciplinary evaluation and detailed observation of the child led to the diagnosis of gratification behavior. That the episodes could be interrupted by distraction, occurred more frequently in isolation, and were associated with perineal stimulation was strongly indicative of gratification syndrome.[4] Her dose of Levetiracetam was gradually tapered. Tablet Clobazam 2.5 mg at bedtime was introduced for its anxiolytic and sedative properties. Parents were also counselled regarding the non-pathological nature of the behavior, the importance of non-punitive distraction techniques, structured playtime, and environmental modification.On follow-up after 4 weeks, a marked reduction in the frequency of episodes was observed. The parents reported improved understanding and better management at home. The child continued to do well in speech therapy and showed no new symptoms suggestive of seizure recurrence.

Video 1:

Video 1:Gratification syndrome

Video available on: https://doi.org/10.25259/ABMH_44_2025

DISCUSSION

Gratification behavior in young children is a diagnostic challenge due to its diverse and non-genital presentations.[1,5] Girls, in particular, may exhibit posturing, grunting, limb stiffening, and even rubbing objects on the perineum without overt self-touch. Misinterpretation as epilepsy is common, especially when there is a coexisting history suggestive of seizures, as in this case.[6] Multiple studies have emphasized that the hallmark feature of gratification syndrome is the presence of consciousness during episodes and cessation upon distraction.[7] Unlike seizures, these episodes are not associated with EEG changes, and post-event confusion or physical exhaustion is usually absent. Misdiagnosis can lead to overmedication, stigmatization, and unnecessary anxiety in caregivers. Educating parents about the benign nature of the behavior, setting firm but gentle behavioral limits, and ensuring the child receives adequate stimulation and attention can effectively manage the condition. In rare cases where symptoms are distressing or disruptive, short-term pharmacological intervention (e.g., with benzodiazepines) may be considered.[8-10]

CONCLUSION

Gratification syndrome should be considered in the differential diagnosis of seizure-like episodes in young children, especially when episodes occur in isolation, are behaviorally driven, and the EEG remains normal. Early recognition and appropriate psychoeducation can prevent misdiagnosis, reduce unnecessary interventions, and alleviate caregiver anxiety.

Authors’ contributions:

DM: Study conception and design, data analysis and review; AT: Manuscript preparation, data collection, analysis and interpretation.

Ethical approval:

Institutional Review Board approval is not required.

Declaration of patient consent:

The authors certify that they have obtained all appropriate patient consent.

Conflicts of interest:

Dr. Deepanjali Medhi is on the Editorial Board of the Journal.

Use of artificial intelligence (AI)-assisted technology for manuscript preparation:

The authors confirm that there was no use of artificial intelligence (AI)-assisted technology for assisting in the writing or editing of the manuscript and no images were manipulated using AI.

Financial support and sponsorship: Nil.

References

  1. , , , . Gratification Disorder (“Infantile Masturbation”): A Review. Arch Dis Child. 2004;89:225-6.
    [CrossRef] [PubMed] [Google Scholar]
  2. , , , . Masturbation in Children with Developmental Disabilities. J Pediatr Health Care. 2005;19:173-7.
    [Google Scholar]
  3. , . Gratification Disorder Presenting as a Seizure: A Case Report. J Pediatr Health Care. 1990;4:200-2.
    [Google Scholar]
  4. , , , , , , et al. Sex-Related Behaviors in Children with Autism Spectrum Disorders. J Dev Behav Pediatr. 2014;35:343-51.
    [Google Scholar]
  5. , . Kaplan & Sadock’s Synopsis of Psychiatry. (11th ed). Philadelphia (PA): Lippincott Williams & Wilkins; . p. :44-46.
    [Google Scholar]
  6. , . Gratification Disorder in a Preschool Girl Masquerading as Seizures. Indian J Psychol Med. 2012;34:386-7.
    [Google Scholar]
  7. , , . Infantile Gratification Behavior Misdiagnosed as Epilepsy: A Case Report. J Pediatr Neurosci. 2017;12:91-3.
    [Google Scholar]
  8. , , , . Seizure or not? Gratification Behavior in a 3-year-old Girl. Neurosciences (Riyadh). 2018;23:236-8.
    [Google Scholar]
  9. , , . Gratification Behavior Mimicking Seizure Disorder: Need for Awareness. Indian J Child Health. 2020;7:114-6.
    [Google Scholar]
  10. , . PPediatric Behavioral Neurology : A Diagnostic Approach. Semin Neurol. 2001;21:65-73.
    [Google Scholar]
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