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Case Reports
. 2019 Aug;39(9):806-810.
doi: 10.1002/pd.5424. Epub 2019 Feb 20.

Prenatal presentation of Aicardi-Goutières syndrome: Nonspecific phenotype necessitates exome sequencing for definitive diagnosis

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Case Reports

Prenatal presentation of Aicardi-Goutières syndrome: Nonspecific phenotype necessitates exome sequencing for definitive diagnosis

Nicolas Bourgon et al. Prenat Diagn. 2019 Aug.
No abstract available

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References

REFERENCES

    1. Crow YJ, Chase DS, Lowenstein Schmidt J, et al. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1. Am J Med Genet A. 2015 Feb;167A(2):296-312.
    1. Desanges C, Lebon P, Bauman C, et al. Elevated interferon-alpha in fetal blood in the prenatal diagnosis of Aicardi-Goutières syndrome. Fetal Diagn Ther. 2006;21(1):153-155.
    1. Le Garrec M, Doret M, Pasquier JC, et al. Prenatal diagnosis of Aicardi-Goutières syndrome. Prenat Diagn. 2005 Jan;25(1):28-30.
    1. Stewart Z, Molin A, Leporrier N, et al. Prenatal diagnosis of Aicardi-Goutières syndrome: a sonographic mimicry of cytomegalovirus fetopathy. J Ultrasound Med Off J Am Inst Ultrasound Med. 2015 Jan;34(1):169-171.
    1. Briggs TA, Wolf NI, D'Arrigo S, et al. Band-like intracranial calcification with simplified gyration and polymicrogyria: a distinct “pseudo-TORCH” phenotype. Am J Med Genet A. 2008 Dec 15;146A(24):3173-3180.

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