HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Optic neuropathy in late-onset neurodegenerative Chédiak-Higashi syndrome.

AbstractBACKGROUND:
The classic form of Chédiak-Higashi syndrome (CHS), an autosomal recessive disorder of lysosomal trafficking with childhood onset caused by mutations in ITALIC! LYST, is typified ophthalmologically by ocular albinism with vision loss attributed to foveal hypoplasia or nystagmus. Optic nerve involvement and ophthalmological manifestations of the late-onset neurodegenerative form of CHS are rarely reported and poorly detailed.
METHODS:
Case series detailing ophthalmological and neurological findings in three adult siblings with the late-onset form of CHS.
RESULTS:
All three affected siblings lacked features of ocular albinism and demonstrated significant optic nerve involvement as evidenced by loss of colour and contrast vision, central visual field loss, optic nerve pallor, retinal nerve fibre layer thinning by optical coherence tomography (OCT) and abnormal visual evoked potential, with severity corresponding linearly to age of the sibling and severity of neurological disease. Further, unusual prominence of a 'third line' on macular OCT that may be due to abnormal melanosomes was seen in all three siblings and in their father. Neurological involvement included parkinsonism, cerebellar ataxia and spastic paraparesis.
CONCLUSIONS:
This report expands the ophthalmological phenotype of the late-onset neurodegenerative form of CHS to include optic neuropathy with progressive vision loss, even in the absence of ocular albinism, and abnormal prominence of the interdigitation zone between cone outer segment tips and apical processes of retinal pigment epithelium cells on macular OCT.
AuthorsNinad Desai, James D Weisfeld-Adams, Scott E Brodie, Catherine Cho, Christine A Curcio, Fred Lublin, Janet C Rucker
JournalThe British journal of ophthalmology (Br J Ophthalmol) Vol. 100 Issue 5 Pg. 704-7 (May 2016) ISSN: 1468-2079 [Electronic] England
PMID26307451 (Publication Type: Journal Article)
CopyrightPublished by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/
Topics
  • Adult
  • Chediak-Higashi Syndrome (complications, diagnosis)
  • Evoked Potentials, Visual
  • Female
  • Humans
  • Male
  • Optic Nerve Diseases (diagnosis, etiology)
  • Phenotype
  • Siblings
  • Tomography, Optical Coherence
  • Vision Disorders (physiopathology)
  • Visual Acuity (physiology)
  • Visual Fields (physiology)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: