Phenotypic characterization of hypomyelination and congenital cataract
- PMID: 17683097
- DOI: 10.1002/ana.21175
Phenotypic characterization of hypomyelination and congenital cataract
Abstract
Objective: To define the clinical and laboratory findings in a novel autosomal recessive white matter disorder called hypomyelination and congenital cataract, recently found to be caused by a deficiency of a membrane protein, hyccin, encoded by the DRCTNNB1A gene located on chromosome 7p21.3-p15.3.
Methods: We performed neurological examination, neurophysiological, neuroimaging, and neuropathological studies on sural nerve biopsy in 10 hypomyelination and congenital cataract patients from 5 unrelated families.
Results: The clinical picture was characterized by bilateral congenital cataract, developmental delay, and slowly progressive neurological impairment with spasticity, cerebellar ataxia, and mild-to-moderate mental retardation. Neurophysiological studies showed a slightly to markedly slowed motor nerve conduction velocity in 9 of 10 patients, and multimodal evoked potentials indicated increased central conduction times. Neuroimaging studies demonstrated a diffuse supratentorial hypomyelination, with in some patients, additional areas of more prominent signal change in the frontal region. Sural nerve biopsy showed a slight-to-severe reduction in myelinated fiber density, with several axons surrounded by a thin myelin sheath or devoid of myelin.
Interpretation: Hypomyelination and congenital cataract is a novel autosomal recessive white matter disorder characterized by the unique association of congenital cataract and hypomyelination of the central and peripheral nervous system.
Comment in
-
Myelin mishaps.Ann Neurol. 2007 Aug;62(2):107-9. doi: 10.1002/ana.21165. Ann Neurol. 2007. PMID: 17683086 No abstract available.
Similar articles
-
Hypomyelination and congenital cataract: neuroimaging features of a novel inherited white matter disorder.AJNR Am J Neuroradiol. 2008 Feb;29(2):301-5. doi: 10.3174/ajnr.A0792. Epub 2007 Nov 1. AJNR Am J Neuroradiol. 2008. PMID: 17974614 Free PMC article.
-
Hypomyelination and congenital cataract: identification of novel mutations in two unrelated families.Eur J Paediatr Neurol. 2013 Jan;17(1):108-11. doi: 10.1016/j.ejpn.2012.06.004. Epub 2012 Jun 30. Eur J Paediatr Neurol. 2013. PMID: 22749724
-
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract.Nat Genet. 2006 Oct;38(10):1111-3. doi: 10.1038/ng1870. Epub 2006 Sep 3. Nat Genet. 2006. PMID: 16951682
-
Hypomyelination and congenital cataract: broadening the clinical phenotype.Arch Neurol. 2011 Sep;68(9):1191-4. doi: 10.1001/archneurol.2011.201. Arch Neurol. 2011. PMID: 21911699 Review.
-
Hypomyelination and Congenital Cataract: Clinical, Imaging, and Genetic Findings in Three Tunisian Families and Literature Review.Neuropediatrics. 2021 Aug;52(4):302-309. doi: 10.1055/s-0041-1728654. Epub 2021 Jun 30. Neuropediatrics. 2021. PMID: 34192786 Review.
Cited by
-
Inherited and acquired disorders of myelin: The underlying myelin pathology.Exp Neurol. 2016 Sep;283(Pt B):452-75. doi: 10.1016/j.expneurol.2016.04.002. Epub 2016 Apr 9. Exp Neurol. 2016. PMID: 27068622 Free PMC article. Review.
-
Hyccin, the molecule mutated in the leukodystrophy hypomyelination and congenital cataract (HCC), is a neuronal protein.PLoS One. 2012;7(3):e32180. doi: 10.1371/journal.pone.0032180. Epub 2012 Mar 26. PLoS One. 2012. PMID: 22461884 Free PMC article.
-
First description of novel compound heterozygous mutations in HYCC1: clinical evaluations and molecular analysis in patient with hypomyelinating leukodystrophy-5 with retrospective view.J Hum Genet. 2025 Feb;70(2):75-85. doi: 10.1038/s10038-024-01300-2. Epub 2024 Oct 28. J Hum Genet. 2025. PMID: 39468300
-
Hypomyelination and Congenital Cataract: Three Siblings Presentation.J Pediatr Neurosci. 2020 Jul-Sep;15(3):270-273. doi: 10.4103/jpn.JPN_161_18. Epub 2020 Nov 6. J Pediatr Neurosci. 2020. PMID: 33531944 Free PMC article.
-
The leukodystrophy protein FAM126A (hyccin) regulates PtdIns(4)P synthesis at the plasma membrane.Nat Cell Biol. 2016 Jan;18(1):132-8. doi: 10.1038/ncb3271. Epub 2015 Nov 16. Nat Cell Biol. 2016. PMID: 26571211 Free PMC article.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical