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Related Experiment Video

Updated: Feb 24, 2026

Handwriting Analysis Indicates Spontaneous Dyskinesias in Neuroleptic Na&#239;ve Adolescents at High Risk for Psychosis
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Ataxia in a Young Female.

R Jayanthi1, K Monica1, K Raja1

  • 1Govt. Stanley Medical College, General Medicine Department, Chennai, Tamil Nadu.

The Journal of the Association of Physicians of India
|August 12, 2017
PubMed
Summary

Neurofibromatosis type 2 (NF2) is a rare genetic disorder causing central nervous system tumors. Early consideration of NF2 is crucial for ataxia with hearing loss.

Area of Science:

  • Genetics
  • Neurology
  • Oncology

Background:

  • Neurofibromatosis type 2 (NF2) is an uncommon genetic disorder.
  • It is characterized by central nervous system tumors, primarily bilateral vestibular schwannomas.
  • Peripheral manifestations like cataracts and cutaneous neurofibromas can also occur.

Observation:

  • This report details a classical case of NF2 with significant clinical symptoms.
  • Characteristic neuroimaging findings supported the diagnosis.
  • The case presentation is accompanied by a review of relevant literature.

Findings:

  • The described NF2 case exhibited florid clinical manifestations.
  • Neuroimaging confirmed the typical features of the disorder.
  • Literature review provides context for this rare condition.

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Implications:

  • NF2 diagnosis requires consideration in patients with ataxia and sensory neural hearing loss.
  • This case highlights the importance of differential diagnosis in neurological presentations.
  • Understanding NF2's varied manifestations is key for timely intervention.