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4H syndrome: a rare cause of leukodystrophy

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References

  1. Atrouni S, Darazé A, Tamraz J, Cassia A, Caillaud C, Mégarbané A (2003) Leukodystrophy associated with oligodontia in a large inbred family: fortuitous association or new entity? Am J Med Genet 118A:76–80

    Article  PubMed  Google Scholar 

  2. Bekiesinska-Figatowska M, Mierzewska h, Kuczynska-Zardzewialy A, Szczepanik E, Obersztyn E (2009) Hypomyelination, hypogonadotropic hypogonadism, hypodontia—first Polish patient. Brain Dev (in press)

  3. Sasaki M, Takanashi JI, Tada H, Sakuma H, Furushima W, Sato N (2009) Diffuse cerebral hypomyelination with cerebellar atrophy and hypoplasia of the corpus callosum. Brain Dev 31:582–587

    Article  PubMed  Google Scholar 

  4. Timmons M, Tsokos M, Abu Asab M, Seminara SB, Zirzow GC, Kaneski CR, Heiss JD, van der Knaap MS, Vanier MT, Schiffmann R, Wong K (2006) Peripheral and central hypomyelination with hypogonadotropic hypogonadism and hypodontia. Neurology 67:2066–2069

    Article  CAS  PubMed  Google Scholar 

  5. Vazquez-Lopez M, Ruiz-Martin Y, de Castro-Castro P, Garzo-fernandez C, Martin-del-Valle F, Marquez-de la Plata L (2008) Central hypomyelination, hypogonadotrophic hypogonadism and hypodontia: a new leukodystrophy. Rev Neurol 47:204–208

    CAS  PubMed  Google Scholar 

  6. Wolf NI, Harting I, Boltshauser E, Wiegand G, Koch J, Schmitt-Mechelke T, Martin E, Zschocke J, Uhlenberg B, Hoffmann GF, Weber L, Ebinger F, Rating D (2005) Leukoencephalopathy with ataxia, hypodontia, and hypomyelination. Neurology 64:1461–1464

    CAS  PubMed  Google Scholar 

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Correspondence to Olivier Outteryck.

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Outteryck, O., Devos, D., Jissendi, P. et al. 4H syndrome: a rare cause of leukodystrophy. J Neurol 257, 1759–1761 (2010). https://doi.org/10.1007/s00415-010-5598-0

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  • DOI: https://doi.org/10.1007/s00415-010-5598-0

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