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February 1, 2008PEDIATRICS

Recognition and Diagnosis of Mucopolysaccharidosis II (Hunter Syndrome)

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Authors

RMRick MartinMBMichael BeckCEChristine M. Eng

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Martin et al. (2008) studied this question.

synapsesocial.com/papers/6a8aec1ade5ec4e001e3ab2chttps://doi.org/10.1542/peds.2007-1350
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Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Hearing Loss in Hunterʼs Syndrome-Mucopolysaccnaridosis II1984 · 37 citations
  2. 2Molecular and phenotypic variation in patients with severe Hunter syndrome1997 · 78 citations
  3. 3Macrocephaly, epilepsy, autism, dysmorphic features, and mental retardation in two sisters: a new autosomal recessive syndrome?1997 · 30 citations
  4. 4Airway changes in children with mucopolysaccharidoses. CT evaluation2002 · 74 citations