Literature DB >> 29479262

Increasing incidence of optic nerve hypoplasia/septo-optic dysplasia spectrum: Geographic clustering in Northern Canada.

Tanya Khaper1, Martin Bunge2, Ian Clark3, Mubeen Fatima Rafay4, Aziz Mhanni5, Nicole Kirouac6, Atul Sharma7, Celia Rodd6, Brandy Wicklow6.   

Abstract

INTRODUCTION: Owing to the shared embryonic origin, defects in development of optic nerves are often seen in conjunction with defects affecting the surrounding brain and pituitary gland. Optic nerve hypoplasia (ONH) and septo-optic dysplasia (SOD) represent a clinical spectrum associated with visual, pituitary and severe central nervous system structural abnormalities (SODplus). Based on changing clinical patterns, our primary objective was to examine trends in annual incidence of ONH/SOD and geographical clustering in Manitoba.
METHODS: This was a retrospective 1996 to 2015 chart review with extraction of anthropometric measures, radiologic findings, parental characteristics, endocrinopathies and neurologic symptoms from all involved in care. Postal codes were used to assign map co-ordinates and identify relevant census-based deprivation indices.
RESULTS: Ninety-three children were identified in our catchment area; Poisson regression confirmed a striking 1.11-fold annual increase (95% confidence interval 1.07 to 1.16) or ~800% over two decades. The annual incidence (averaged 2010 to 2014 chart data) reached 53.3 per 100,000, affecting 1 in 1875 live births. Most (~55%) had SODplus. Common presenting features were hypoglycemia, nystagmus, seizures and developmental delay; 40% had hormone deficiencies; 80% had reduced visual acuity, typically bilateral. Many were premature with young, primiparous mothers. Unhealthy maternal lifestyles and severe material deprivation were noted. There was disproportionate clustering in individuals from Northern Manitoba at three times the average provincial rate.
CONCLUSION: We noted a dramatic rise in the annual incidence of ONH/SOD, which was strongly associated with poverty and northern communities. The pattern was consistent with environmental or nutritional etiologies. Many children were severely affected with increased morbidity and health care burdens.

Entities:  

Keywords:  Blindness; Hypopituitarism; Incidence; Poverty; Septo-optic dysplasia

Year:  2017        PMID: 29479262      PMCID: PMC5804768          DOI: 10.1093/pch/pxx118

Source DB:  PubMed          Journal:  Paediatr Child Health        ISSN: 1205-7088            Impact factor:   2.253


  16 in total

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2.  Geographical distribution of optic nerve hypoplasia and septo-optic dysplasia in Northwest England.

Authors:  Leena Patel; Richard J Q McNally; Elizabeth Harrison; I Christopher Lloyd; Peter E Clayton
Journal:  J Pediatr       Date:  2006-01       Impact factor: 4.406

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Journal:  J AAPOS       Date:  1999-02       Impact factor: 1.220

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Journal:  Alcohol Clin Exp Res       Date:  2011-02-17       Impact factor: 3.455

5.  Septo-optic dysplasia plus: a spectrum of malformations of cortical development.

Authors:  S P Miller; M I Shevell; Y Patenaude; C Poulin; A M O'Gorman
Journal:  Neurology       Date:  2000-04-25       Impact factor: 9.910

6.  Mutations in the homeobox gene HESX1/Hesx1 associated with septo-optic dysplasia in human and mouse.

Authors:  M T Dattani; J P Martinez-Barbera; P Q Thomas; J M Brickman; R Gupta; I L Mårtensson; H Toresson; M Fox; J K Wales; P C Hindmarsh; S Krauss; R S Beddington; I C Robinson
Journal:  Nat Genet       Date:  1998-06       Impact factor: 38.330

7.  Optic nerve hypoplasia: Risk factors and epidemiology.

Authors:  Kristina Tornqvist; Anders Ericsson; Bengt Källén
Journal:  Acta Ophthalmol Scand       Date:  2002-06

8.  Endocrine and pubertal disturbances in optic nerve hypoplasia, from infancy to adolescence.

Authors:  Oliver J Oatman; Donald R McClellan; Micah L Olson; Pamela Garcia-Filion
Journal:  Int J Pediatr Endocrinol       Date:  2015-04-15

9.  Gastroschisis Complicated by Septo-Optic Dysplasia: Two Distinct Anomalies with a Common Origin.

Authors:  Jodi Garvin; Venkatesh Sampath; Vijender R Karody
Journal:  AJP Rep       Date:  2015-10-16

10.  HESX1 mutations are an uncommon cause of septooptic dysplasia and hypopituitarism.

Authors:  David E G McNay; James P Turton; Daniel Kelberman; Kathryn S Woods; Raja Brauner; Anastasios Papadimitriou; Eberhard Keller; Alexandra Keller; Nele Haufs; Heiko Krude; Stephen M Shalet; Mehul T Dattani
Journal:  J Clin Endocrinol Metab       Date:  2006-12-05       Impact factor: 5.958

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5.  Hypernatremia in an Infant: A Case of Septo-Optic Dysplasia.

Authors:  Oluwatosin O Oyadiran; Naxdaris Gonzalez; Ahmad Khiami
Journal:  Cureus       Date:  2021-01-03

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