Patients with autosomal-recessive osteopetrosis presenting with hydrocephalus and hindbrain posterior fossa crowding

J Neurosurg Pediatr. 2008 Jan;1(1):103-6. doi: 10.3171/PED-08/01/103.

Abstract

Osteopetrosis is a heterogeneous group of disorders characterized by abnormal bone sclerosis. As a result, patients often require input regarding various neurological complications. Although autosomal-recessive osteopetrosis has been associated with hydrocephalus, it has not been linked to hindbrain abnormalities. The authors present 3 cases of auto-somal-recessive osteopetrosis in patients who presented with hydrocephalus. In each of these patients, cerebrospinal fluid diversion procedures were required and hindbrain compression developed. To date, only 1 patient has needed craniocervical decompression due to symptomatic brainstem compression.

Publication types

  • Case Reports

MeSH terms

  • Cerebrospinal Fluid Shunts
  • Child
  • Chromosome Disorders / genetics*
  • Cranial Fossa, Posterior / pathology*
  • Decompression, Surgical
  • Female
  • Humans
  • Hydrocephalus* / complications
  • Hydrocephalus* / diagnosis
  • Hydrocephalus* / surgery
  • Magnetic Resonance Imaging
  • Optic Nerve Diseases / diagnosis
  • Optic Nerve Diseases / etiology
  • Optic Nerve Diseases / surgery
  • Osteopetrosis* / complications
  • Osteopetrosis* / genetics
  • Osteopetrosis* / pathology
  • Rhombencephalon / diagnostic imaging
  • Rhombencephalon / pathology*
  • Rhombencephalon / surgery
  • Syringomyelia / diagnosis
  • Syringomyelia / etiology
  • Syringomyelia / surgery
  • Tomography, X-Ray Computed