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[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.
Abstract:
A 4-month-old girl developed convulsion in the neonatal period, which was focal motor seizures in the initial stage and later became spasm and tonic spasm. And the girl also had psychomotor retardation and recurrent pulmonary infection. Electroencephalography showed hypsarrhythmia, normal results were obtained from cranial magnetic resonance imaging, cerebrospinal fluid examination, and urine organic acid analysis, as well as the spectral analyses of blood ammonia, blood lactic acid, blood amino acids, and acylcarnitines. Gene detection revealed a de novo heterozygous mutation, c.607G>A (p.G203R) , in GNAO1. The girl was then diagnosed with GNAO1-associated early infantile epileptic encephalopathy (EIEE type 17). The seizures were well controlled by topiramate and vigabatrin, but there was no improvement in psychomotor development. She also suffered from recurrent pulmonary infection and died at the age of 12 months due to severe pneumonia. For children with unexplained early infantile epileptic encephalopathy, GNAO1 gene mutations should be considered and genetic tests should be performed as early as possible. Recurrent pulmonary infection should also be taken seriously.
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