Literature DB >> 28177849

The clinical evaluation of infantile nystagmus: What to do first and why.

Morgan Bertsch1, Michael Floyd1,2, Taylor Kehoe1,3, Wanda Pfeifer1, Arlene V Drack1.   

Abstract

INTRODUCTION: Infantile nystagmus has many causes, some life threatening. We determined the most common diagnoses in order to develop a testing algorithm.
METHODS: Retrospective chart review. Exclusion criteria were no nystagmus, acquired after 6 months, or lack of examination. DATA COLLECTED: pediatric eye examination findings, ancillary testing, order of testing, referral, and final diagnoses. Final diagnosis was defined as meeting published clinical criteria and/or confirmed by diagnostic testing. Patients with a diagnosis not meeting the definition were "unknown." Patients with incomplete testing were "incomplete." Patients with multiple plausible etiologies were "multifactorial." Patients with negative complete workup were "motor."
RESULTS: A total of 284 charts were identified; 202 met inclusion criteria. The three most common causes were Albinism (19%), Leber Congenital Amaurosis (LCA; 14%), and Non-LCA retinal dystrophy (13%). Anatomic retinal disorders comprised 10%, motor another 10%. The most common first test was MRI (74/202) with a diagnostic yield of 16%. For 28 MRI-first patients, nystagmus alone was the indication; for 46 MRI-first patients other neurologic signs were present. 0/28 nystagmus-only patients had a diagnostic MRI while 14/46 (30%) with neurologic signs did. The yield of ERG as first test was 56%, OCT 55%, and molecular genetic testing 47%. Overall, 90% of patients had an etiology identified.
CONCLUSION: The most common causes of infantile nystagmus were retinal disorders (56%), however the most common first test was brain MRI. For patients without other neurologic stigmata complete pediatric eye examination, ERG, OCT, and molecular genetic testing had a higher yield than MRI scan. If MRI is not diagnostic, a complete ophthalmologic workup should be pursued.

Entities:  

Keywords:  Electroretinogram; magnetic resonance imaging; nystagmus

Mesh:

Year:  2017        PMID: 28177849      PMCID: PMC5665016          DOI: 10.1080/13816810.2016.1266667

Source DB:  PubMed          Journal:  Ophthalmic Genet        ISSN: 1381-6810            Impact factor:   1.803


  46 in total

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2.  Photoaversion in Leber's congenital amaurosis.

Authors:  E I Traboulsi; I H Maumenee
Journal:  Ophthalmic Genet       Date:  1995-03       Impact factor: 1.803

3.  Clinical and ocular motor analysis of the infantile nystagmus syndrome in the first 6 months of life.

Authors:  R W Hertle; V K Maldanado; M Maybodi; D Yang
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4.  Novel FRMD7 Mutations and Genomic Rearrangement Expand the Molecular Pathogenesis of X-Linked Idiopathic Infantile Nystagmus.

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5.  Eye movement abnormalities in Joubert syndrome.

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Authors:  Pei-Wen Chiang; Elaine Spector; Tracy L McGregor
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Review 7.  Nystagmus in childhood.

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Journal:  Pediatr Neonatol       Date:  2014-07-31       Impact factor: 2.083

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Authors:  Gregory D Kiblinger; Billi S Wallace; Mujahid Hines; R Michael Siatkowski
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9.  Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus.

Authors:  Patrick Tarpey; Shery Thomas; Nagini Sarvananthan; Uma Mallya; Steven Lisgo; Chris J Talbot; Eryl O Roberts; Musarat Awan; Mylvaganam Surendran; Rebecca J McLean; Robert D Reinecke; Andrea Langmann; Susanne Lindner; Martina Koch; Sunila Jain; Geoffrey Woodruff; Richard P Gale; Andrew Bastawrous; Chris Degg; Konstantinos Droutsas; Ioannis Asproudis; Alina A Zubcov; Christina Pieh; Colin D Veal; Rajiv D Machado; Oliver C Backhouse; Laura Baumber; Cris S Constantinescu; Michael C Brodsky; David G Hunter; Richard W Hertle; Randy J Read; Sarah Edkins; Sarah O'Meara; Adrian Parker; Claire Stevens; Jon Teague; Richard Wooster; P Andrew Futreal; Richard C Trembath; Michael R Stratton; F Lucy Raymond; Irene Gottlob
Journal:  Nat Genet       Date:  2006-10-01       Impact factor: 38.330

10.  The Role of FRMD7 in Idiopathic Infantile Nystagmus.

Authors:  Rachel J Watkins; Mervyn G Thomas; Chris J Talbot; Irene Gottlob; Sue Shackleton
Journal:  J Ophthalmol       Date:  2011-08-29       Impact factor: 1.909

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2.  Presentation of TRPM1-Associated Congenital Stationary Night Blindness in Children.

Authors:  Virginia Miraldi Utz; Wanda Pfeifer; Susannah Q Longmuir; Richard John Olson; Kai Wang; Arlene V Drack
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Review 3.  Ocular manifestations in patients with inborn errors of intracellular cobalamin metabolism: a systematic review.

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4.  Ocular evaluation and genetic test for an early Alström Syndrome diagnosis.

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5.  TUBB3 M323V Syndrome Presents with Infantile Nystagmus.

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7.  Nystagmus in Down Syndrome - a Retrospective Notes Review.

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8.  Cross-sectional observational analysis of the genetic referral practices across pediatric ophthalmology outpatient departments in an urban setting.

Authors:  Shruti Bajaj; Mathangi Venkatraman; Nidhi Agarwal; Mihir Kothari
Journal:  Indian J Ophthalmol       Date:  2022-07       Impact factor: 2.969

9.  Post audio-visual biofeedback training visual functions and quality of life in paediatric idiopathic infantile nystagmus: A pilot study.

Authors:  Monica Daibert-Nido; Yulia Pyatova; Michelle Markowitz; Maryam Taheri-Shirazi; Samuel N Markowitz
Journal:  Eur J Ophthalmol       Date:  2021-01-26       Impact factor: 2.597

  9 in total

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