Phenotypic characterization of hypomyelination and congenital cataract

Ann Neurol. 2007 Aug;62(2):121-7. doi: 10.1002/ana.21175.

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.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biopsy
  • Cataract / complications
  • Cataract / congenital*
  • Cataract / genetics
  • Cataract / physiopathology*
  • Cerebellar Ataxia / etiology
  • Demyelinating Diseases / complications
  • Demyelinating Diseases / genetics
  • Demyelinating Diseases / physiopathology*
  • Female
  • Genes, Recessive
  • Hereditary Central Nervous System Demyelinating Diseases / complications
  • Hereditary Central Nervous System Demyelinating Diseases / diagnosis
  • Hereditary Central Nervous System Demyelinating Diseases / genetics
  • Hereditary Central Nervous System Demyelinating Diseases / physiopathology*
  • Humans
  • Intellectual Disability / etiology
  • Intracellular Signaling Peptides and Proteins / deficiency
  • Magnetic Resonance Imaging*
  • Male
  • Membrane Proteins / deficiency
  • Muscle Spasticity / etiology
  • Nervous System / pathology
  • Nervous System / physiopathology
  • Neural Conduction
  • Peripheral Nervous System Diseases / complications
  • Peripheral Nervous System Diseases / genetics
  • Peripheral Nervous System Diseases / physiopathology*
  • Phenotype
  • Retrospective Studies
  • Single-Blind Method
  • Sural Nerve / pathology

Substances

  • FAM126A protein, human
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins