Literature DB >> 30196776

Ophthalmoplegia and Congenital Cranial Dysinnervation Disorders.

Darren T Oystreck1,2,3.   

Abstract

Some forms of ophthalmoplegia are congenital and fall into the category of Congenital Cranial Dysinnervation Disorders (CCDDs). These disorders arise from a primary defect of cranial nucleus/nerve development or guidance. Many have substantial limitations of ocular motility with or without other associated features. The type and degree of ophthalmoplegia can be similar between CCDD subtypes as well as with non-congenital forms of ophthalmoplegia. Therefore diagnostic confirmation often requires neuro-imaging and/or genetic investigations. The clinician should consider this category in cases of ophthalmoplegia that are congenital and nonprogressive in nature.

Entities:  

Keywords:  Congenital cranial dysinnervation disorders; HOXA1 syndrome; Moebius syndrome; congenital; congenital fibrosis of the extraocular muscles; horizontal gaze palsy and progressive scoliosis; ophthalmoplegia

Mesh:

Year:  2018        PMID: 30196776     DOI: 10.1080/2576117X.2017.1416242

Source DB:  PubMed          Journal:  J Binocul Vis Ocul Motil        ISSN: 2576-117X


  1 in total

1.  Clinical Characteristics and Surgical Outcomes of Patients with Congenital Fibrosis of the Superior Rectus Muscle.

Authors:  Min Yang; Licheng Fu; Jianhua Yan
Journal:  Ophthalmol Ther       Date:  2022-03-13
  1 in total

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