Unveiling Fahr's Syndrome in a Child: A Case Linked to Congenital Hypoparathyroidism

Ghizlane Kassal1, Rabiy Elqadiri1, Soumia Mghar1

  • 1Mother and Child Department, General Pediatrics, University Hospital Center, Mohammed VI, Marrakech, MAR.

Cureus
|June 13, 2025
PubMed

Insights

Fahr's syndrome, a rare neurological disorder causing brain calcifications, can be linked to hypoparathyroidism in children. Early diagnosis using clinical markers and CT scans is crucial for effective management.

Area of Science:

  • Neurology
  • Pediatrics
  • Radiology

Background:

  • Fahr's syndrome is a rare neurological disorder characterized by abnormal calcium deposits in the brain.
  • It can stem from hormonal imbalances, genetic factors, CNS infections, or toxic exposures.

Observation:

  • A pediatric case of Fahr's syndrome associated with hypoparathyroidism is presented.
  • The patient exhibited seizures and developmental delays.

Findings:

  • Clinical suspicion was raised by patient history, symptoms, and lab results.
  • Cerebral computed tomography (CT) confirmed brain calcifications, diagnosing Fahr's syndrome.

Implications:

  • Early identification of Fahr's syndrome is essential for timely intervention.
  • Clinical and biological markers are vital for diagnosis, supported by imaging.
  • Prompt diagnosis aids in effective patient management and treatment strategies.

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