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Glucose 6-phosphate dehydrogenase deficiency with kernicterus: progressive late recovery from profound deafness

S Akhtar1, M Drenovak, H Bantock

  • 1Royal National Throat Nose and Ear Hospital, London, UK.

Insights

Glucose 6-Phosphate Dehydrogenase (G6-PD) deficiency in infants can cause severe jaundice. This case report highlights a rare instance of significant neurological recovery from Kernicterus in a G6-PD deficient infant.

Area of Science:

  • Neonatology
  • Pediatric Neurology
  • Hematology

Background:

  • Glucose 6-Phosphate Dehydrogenase (G6-PD) deficiency is a common inherited condition.
  • Severe unconjugated hyperbilirubinemia in G6-PD deficiency can lead to kernicterus.

Observation:

  • A near-term infant with G6-PD deficiency presented with extremely high bilirubin levels (703 µmol/L) but maintained stable hemoglobin.
  • At 4 months, the infant showed signs of kernicterus, including profound sensorineural deafness and encephalopathy.

Findings:

  • Remarkable neurological and auditory recovery was observed by 15 months of age.
  • Motor and cerebral signs regressed towards normal, with hearing returning to normal levels.
  • Communication skills showed a 4-6 month delay but were improving.

Implications:

  • This case suggests potential for significant neurodevelopmental recovery even after severe kernicterus in G6-PD deficient infants.
  • Highlights the importance of monitoring neurodevelopmental outcomes in infants with G6-PD deficiency and hyperbilirubinemia.
  • Suggests that early intervention and supportive care may play a role in recovery.

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