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MRI in Smith-Lemli-Opitz syndrome type I

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Abstract

We describe a single case of a polymalformational syndrome in which the MR findings were of great help in the final diagnosis of Smith-Lemli-Opitz syndrome (SLOS) type I. MRI was performed for evaluation of the brain morphology since the clinical and laboratory findings were suggestive but not unequivocally indicative of SLOS. MRI findings of frontal lobe hypoplasia, cortical migration defect, and abnormalities of median line structures prompted the final diagnosis of SLOS.

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References

  1. Aicardi J (1992) Diseases of the nervous system in childwood. MacKeith Press, London, pp 258–259

    Google Scholar 

  2. Cherstvoj ED, Lazjuk GI, Ostrovsakaia TI, et al (1984) The Smith Lemli Opitz syndrome: a detailed pathological study as a clue to etiological heterogeneity. Virchows Arch [A] 404: 413–425

    Article  Google Scholar 

  3. Curry CJR, Carey JC, Holland JS, et al (1987) Smith Lemli Opitz syndrome type II: multiple congenital anomalies with male pseudohermaphrodism and frequent early lethality. Am J Med Genet 26: 45–57

    Article  PubMed  CAS  Google Scholar 

  4. Fierro M, Martinez AJ, Harbison JW (1977) Smith Lemli Opitz syndrome: neuropathological and ophthalmological observations. Dev Med Child Neurol 19: 57–62

    PubMed  CAS  Google Scholar 

  5. Garcia CA, McGarry PA, Voirol M, et al (1973) Neurological involvement in the Smith Lemli Opitz syndrome: clinical and neuropathologic findings. Dev Med Child Neurol 15: 48–55

    PubMed  CAS  Google Scholar 

  6. Hermann TE, Siegel MJ, Lee BCD, et al (1993) Smith Lemli Opitz syndrome type II: report of a case with additional radiographic findings. Pediatr Radiol 23: 37–40

    Article  Google Scholar 

  7. Lachman MF, Wright Y, Witheman DAH, et al (1991) Brief clinical report: a 46 XY phenotypic female with Smith Lemli Opitz syndrome. Clin Genet 39: 136–141

    Article  PubMed  CAS  Google Scholar 

  8. Le Merrer M, Briard ML, Girard S, et al (1988) Lethal acrodysgenital dwarfism: a severe lethal condition resembling Smith Lemli Opitz syndrome. J Med Genet 25: 88–95

    Article  PubMed  CAS  Google Scholar 

  9. Smith DW, Lemli L, Opitz JM (1964) A new recognized syndrome of multiple congenital anomalies. J Pediatr 64: 210–217

    Article  PubMed  CAS  Google Scholar 

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Trasimeni, G., Di Biasi, C., Iannilli, M. et al. MRI in Smith-Lemli-Opitz syndrome type I. Child’s Nerv Syst 13, 47–49 (1997). https://doi.org/10.1007/s003810050039

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  • DOI: https://doi.org/10.1007/s003810050039

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