[Recurrent convulsion and pulmonary infection complicated by psychomotor retardation in an infant]

Juan Xiong1, Jing Peng, Hao-Lin Duan

  • 1Department of Pediatrics, Xiangya Hospital, Central South University, Changsha 410008, China. yf2323@hotmail.com.

Insights

GNAO1 gene mutations cause early infantile epileptic encephalopathy (EIEE type 17), leading to severe developmental delays and fatal infections. Early genetic testing is crucial for unexplained EIEE cases.

Area of Science:

  • Genetics
  • Neurology
  • Pediatrics

Background:

  • Early Infantile Epileptic Encephalopathy (EIEE) presents significant diagnostic challenges.
  • Genetic etiologies are increasingly recognized in unexplained EIEE cases.

Observation:

  • A 4-month-old infant experienced neonatal seizures, progressing to spasms and tonic seizures.
  • The infant exhibited psychomotor retardation and recurrent pulmonary infections.
  • Standard investigations including neuroimaging and metabolic screening were normal.

Findings:

  • Gene sequencing identified a de novo heterozygous GNAO1 mutation (c.607G>A, p.G203R).
  • The patient was diagnosed with GNAO1-associated EIEE (EIEE type 17).
  • Seizure control was achieved with topiramate and vigabatrin, but psychomotor development did not improve.

Implications:

  • GNAO1 gene mutations should be considered in infants with unexplained EIEE.
  • Prompt genetic testing can facilitate early diagnosis and management.
  • Recurrent pulmonary infections in EIEE patients require vigilant monitoring and management.

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