A Rare Case of Aicardi-Goutières Syndrome Who Showed a Positive Evolution after Being Treated with Growth Hormone, High Doses of Melatonin and Neurorehabilitation

@inproceedings{Devesa2017ARC,
  title={A Rare Case of Aicardi-Gouti{\`e}res Syndrome Who Showed a Positive Evolution after Being Treated with Growth Hormone, High Doses of Melatonin and Neurorehabilitation},
  author={Jes{\'u}s Devesa and Alba Alonso and P Porto and Ana Quintana and M Iba{\~n}ez Carrillo and Pablo Martinez Devesa and Carlos Israel Puell},
  year={2017}
}
1) Background: The Aicardi-Goutières syndrome (AGS) is a rare congenital disease which courses with severe psychomotor delay in neurodevelopment. We studied a 3-years and 4months old child with very important growth and weight affectation, microcephaly and loss of his developmental skills from 16-months of age, in which previous metabolic and genetic studies discarded any abnormality. Therefore diagnosis was cerebral palsy of unknown etiology. He presented spastic paraparesia, poor fine… 

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TLDR
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TLDR
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TLDR
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TLDR
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