A case with central and peripheral hypomyelination with hypogonadotropic hypogonadism and hypodontia (4H syndrome) plus cataract

J Neurol Sci. 2011 Jan 15;300(1-2):179-81. doi: 10.1016/j.jns.2010.09.009. Epub 2010 Sep 29.

Abstract

Hypomyelination with hypogonadotropic hypogonadism and hypodontia (4H syndrome) is a rare disease, characterized by both central and peripheral hypomyelination. We describe a 21-year-old male with mildly progressive ataxia, mental retardation, pituitary hypogonadotropic hypogonadism, delayed dentition, and cataract. Brain magnetic resonance imaging showed hypomyelinated white matter, cerebellar atrophy, and a thin corpus callosum. The literature suggests that abnormal findings upon sural nerve biopsy may indicate peripheral hypomyelination, even in the absence of clinically and physiologically evident peripheral neuropathy. A sural nerve biopsy of this patient was normal, and this finding is further discussed. Taken together with previous reports, this case suggests that 4H syndrome can be regarded as a spectrum disorder, the cardinal signs of which may be central hypomyelination, ataxia, hypogonadotropic hypogonadism, and hypodontia.

Publication types

  • Case Reports

MeSH terms

  • Anodontia / complications
  • Anodontia / pathology*
  • Ataxia / complications
  • Ataxia / pathology*
  • Atrophy / pathology
  • Brain / pathology
  • Cataract / complications*
  • Cataract / pathology
  • Demyelinating Diseases / complications
  • Demyelinating Diseases / pathology*
  • Humans
  • Hypogonadism / complications
  • Hypogonadism / pathology*
  • Intellectual Disability / complications
  • Intellectual Disability / pathology*
  • Magnetic Resonance Imaging
  • Male
  • Nerve Fibers, Myelinated / pathology*
  • Sural Nerve / pathology
  • Syndrome
  • Young Adult