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Septo-optic Dysplasia

Assessment of Associated Findings with Special Attention to the Olfactory Sulci and Tracts

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Abstract

Purpose

Septo-optic dysplasia is a congenital disorder consisting of optic nerve hypoplasia and absent septum pellucidum. While associated anomalies have been described, olfactory sulcus and bulb-tract hypoplasia have been scantily reported and was the focus of this study.

Methods

The picture archival and communications system and radiology information system (PACS-RIS) was searched over 15 years for patients with suspected septo-optic dysplasia (n= 41) and cerebral magnetic resonance imaging (MRI). Included patients had coronal (≤3 mm), axial (≤4 mm), and sagittal (≤4 mm) imaging reviewed by two staff neuroradiologists by consensus. Both olfactory sulcus and bulb-tract hypoplasia were ascribed a grade of 0 (normal) to 3 (complete hypoplasia). Other associated congenital anomalies were recorded, if present. Incidence of anomalies were compared to age-matched and gender-matched control patients.

Results

Out of 41 septo-optic dysplasia patients 33 were included (mean age = 120.7 months), with 8 excluded due to isolated septum pellucidum absence (n= 5), isolated bilateral optic hypoplasia (n= 2), or inadequate imaging (n= 1). An olfactory sulcus was hypoplastic on one or both sides in 14/33 (42.4%). Olfactory bulb hypoplasia was noted in one or both tracts in 15/33 (45.4%). A significant correlation was found between degree of olfactory sulcal and bulb-tract hypoplasia (ρ = 0.528, p= 0.0009). Other anomalies were: anterior falx dysplasia (n= 16, 48.5%), incomplete hippocampal inversion (n= 14, 42.4%), polymicrogyria (n= 11, 33.3%), callosal complete or partial agenesis (n = 10, 30.3%), schizencephaly (n = 8, 24.2%), ectopic posterior pituitary (n= 6, 18.2%), and nodular heterotopia (n= 4, 12.1%). Of the age-matched control patients 10/33 (30.3%) had at least mild anterior falx hypoplasia, and 1 control patient was noted to have unilateral incomplete hippocampal inversion (IHI); none of the age-matched control patients had olfactory sulcus or bulb-tract hypoplasia.

Conclusion

Olfactory sulcus and bulb-tract hypoplasia are fairly common in septo-optic dysplasia and can be discordant between sides. Of the other associated anomalies, anterior falx dysplasia seems to be the most common.

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Abbreviations

IHI:

Incomplete hippocampal inversion

PMG:

Polymicrogyria

PVNH:

Periventricular nodular heterotopia

SOD:

Septo-optic dysplasia

SOD-plus:

Septo-optic dysplasia and schizencephaly

References

  1. Bhatnagar S, Kuber R, Shah D, Kulkarni V. Unilateral closed lip schizencephaly with septo-optic dysplasia. Ann Med Health Sci Res. 2014;4:283–5.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Patel L, McNally RJ, Harrison E, Lloyd IC, Clayton PE. Geographical distribution of optic nerve hypoplasia and septo-optic dysplasia in Northwest England. J Pediatr. 2006;148:85–8.

    Article  PubMed  Google Scholar 

  3. Maurya VK, Ravikumar R, Bhatia M, Rai R. Septo-optic dysplasia: Magnetic Resonance Imaging findings. Med J Armed Forces India. 2015;71:287–9.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Kelberman D, Dattani MT. Septo-optic dysplasia—novel insights into the aetiology. Horm Res. 2008;69:257–65.

    Article  CAS  PubMed  Google Scholar 

  5. Salmela MB, Cauley KA, Nickerson JP, Koski CJ, Filippi CG. Magnetic resonance diffusion tensor imaging (MRDTI) and tractography in children with septo-optic dysplasia. Pediatr Radiol. 2010;40:708–13.

    Article  PubMed  Google Scholar 

  6. Kelberman D, Dattani MT. Genetics of septo-optic dysplasia. Pituitary. 2007;10:393–407.

    Article  CAS  PubMed  Google Scholar 

  7. Garcia ML, Ty EB, Taban M, Rothner DA, Rogers D, Traboulsi EI. Systemic and ocular findings in 100 patients with optic nerve hypoplasia. J Child Neurol. 2006;21:949–56.

    Article  PubMed  Google Scholar 

  8. Barkovich AJ, Fram EK, Norman D. Septo-optic dysplasia: MR imaging. Radiology. 1989;171:189–92.

    Article  CAS  PubMed  Google Scholar 

  9. Al-Senawi R, Al-Jabri B, Al-Zuhaibi S, Al-Azri F, Al-Yarubi S, Harikrishna B, Al-Futaisi A, Ganesh A. Septo-optic dysplasia complex: clinical and radiological manifestations in Omani children. Oman J Ophthalmol. 2013;6:193–8.

    Article  PubMed  PubMed Central  Google Scholar 

  10. Kuban KC, Teele RL, Wallman J. Septo-optic-dysplasia-schizencephaly. Radiographic and clinical features. Pediatr Radiol. 1989;19:145–50.

    Article  CAS  PubMed  Google Scholar 

  11. Webb EA, Dattani MT. Septo-optic dysplasia. Eur J Hum Genet. 2010;18:393–7.

    Article  PubMed  Google Scholar 

  12. Miller SP, Shevell MI, Patenaude Y, Poulin C, O’Gorman AM. Septo-optic dysplasia plus: a spectrum of malformations of cortical development. Neurology. 2000;54:1701–3.

    Article  CAS  PubMed  Google Scholar 

  13. Ribeiro M, Machado A, Soares-Fernandes J. Septo-optic dysplasia with olfactory tract hypoplasia. J Pediatr Neurosci. 2009;4:49.

    Article  PubMed  PubMed Central  Google Scholar 

  14. Puche AC, Baker H. Olfactory cell derivation and migration. J Mol Histol. 2007;38:513–5.

    Article  PubMed  Google Scholar 

  15. Riedl SW, Müllner-Eidenböck A, Prayer D, Bernert G, Frisch H. Auxological, ophthalmological, neurological and MRI findings in 25 Austrian patients with septo-optic dysplasia (SOD). Preliminary data. Horm Res. 2002;58(Suppl 3):16–9.

    CAS  PubMed  Google Scholar 

  16. Riedl S, Vosahlo J, Battelino T, Stirn-Kranjc B, Brugger PC, Prayer D, Müllner-Eidenböck A, Kapelari K, Blümel P, Waldhör T, Krasny J, Lebl J, Frisch H. Refining clinical phenotypes in septo-optic dysplasia based on MRI findings. Eur J Pediatr. 2008;167:1269–76.

    Article  PubMed  Google Scholar 

  17. Cemeroglu AP, Coulas T, Kleis L. Spectrum of clinical presentations and endocrinological findings of patients with septo-optic dysplasia: a retrospective study. J Pediatr Endocrinol Metab. 2015;28:1057–63.

    Article  PubMed  Google Scholar 

  18. Alt C, Shevell MI, Poulin C, Rosenblatt B, Saint-Martin C, Srour M. Clinical and radiologic spectrum of septo-optic dysplasia: review of 17 cases. J Child Neurol. 2017;32:797–803.

    Article  PubMed  Google Scholar 

  19. Brodsky MC, Glasier CM. Optic nerve hypoplasia. Clinical significance of associated central nervous system abnormalities on magnetic resonance imaging. Arch Ophthalmol. 1993;111:66–74.

    Article  CAS  PubMed  Google Scholar 

  20. Lambert SR, Hoyt CS, Narahara MH. Optic nerve hypoplasia. Surv Ophthalmol. 1987;32:1–9.

    Article  CAS  PubMed  Google Scholar 

  21. Lubinsky MS. Hypothesis: septo-optic dysplasia is a vascular disruption sequence. Am J Med Genet. 1997;69:235–6.

    Article  CAS  PubMed  Google Scholar 

  22. Stevens CA, Dobyns WB. Septo-optic dysplasia and amniotic bands: further evidence for a vascular pathogenesis. Am J Med Genet A. 2004;125A:12–6.

    Article  PubMed  Google Scholar 

  23. Manara R, Salvalaggio A, Favaro A, Palumbo V, Citton V, Elefante A, Brunetti A, Di Salle F, Bonanni G, Sinisi AA; Kallmann Syndrome Neuroradiological Study Group. Brain changes in Kallmann syndrome. AJNR Am J Neuroradiol. 2014;35:1700–6.

    Article  PubMed  Google Scholar 

  24. Truwit CL, Barkovich AJ, Grumbach MM, Martini JJ. MR imaging of Kallmann syndrome, a genetic disorder of neuronal migration affecting the olfactory and genital systems. AJNR Am J Neuroradiol. 1993;14:827–38.

    CAS  PubMed  Google Scholar 

  25. Bossy J. Development of olfactory and related structures in staged human embryos. Anat Embryol (Berl). 1980;161:225–36.

    Article  CAS  Google Scholar 

  26. Favre JJ, Chaffanjon P, Passagia JG, Chirossel JP. Blood supply of the olfactory nerve. Meningeal relationships and surgical relevance. Surg Radiol Anat. 1995;17:133–8. 12–4.

    Article  CAS  PubMed  Google Scholar 

  27. Signorini SG, Decio A, Fedeli C, Luparia A, Antonini M, Bertone C, Misefari W, Ruberto G, Bianchi PE, Balottin U. Septo-optic dysplasia in childhood: the neurological, cognitive and neuro-ophthalmological perspective. Dev Med Child Neurol. 2012;54(11):1018–24.

    Article  PubMed  Google Scholar 

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Correspondence to John C. Benson.

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Conflict of interest

J.C. Benson, D. Nascene, C. Truwit and A.M. McKinney declare that they have no competing interests.

Ethical standards

Institutional Review Board (IRB) approval was obtained for this retrospective study.

Additional information

This article is not under consideration for publication elsewhere. All authors have participated sufficiently to take public responsibility for content. No external funding was used for the preparation of this manuscript.

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Benson, J.C., Nascene, D., Truwit, C. et al. Septo-optic Dysplasia. Clin Neuroradiol 29, 505–513 (2019). https://doi.org/10.1007/s00062-018-0687-z

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  • DOI: https://doi.org/10.1007/s00062-018-0687-z

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