HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Stabilization of juvenile metachromatic leukodystrophy after bone marrow transplantation: a 13-year follow-up.

Abstract
A 29-year-old female patient with juvenile metachromatic leukodystrophy diagnosed at age 14 years received a bone marrow transplant at age 16 years. A report was published 6 years after bone marrow transplantation concluding that the disease had slowly progressed in the 2 years following bone marrow transplantation. We now report on a further 7-year follow-up, typified by a steady state of spastic paraplegia and mild dementia. Neurophysiological, neuroradiological, and psychological status also remained stable. In the patient's leukocytes, the activity of arylsulfatase A, the enzyme deficient in untreated metachromatic leukodystrophy, was within the normal range whereas urinary sulfatides remained elevated. Data on the natural course of juvenile metachromatic leukodystrophy are rare, so in the present case it is difficult to establish whether the rather favorable course can be attributed with certainty to bone marrow transplantation. The long-term stabilization in this patient, however, suggested that bone marrow transplantation may halt the progression of juvenile metachromatic leukodystrophy.
AuthorsMaria Görg, Wanja Wilck, Barbara Granitzny, Anne Suerken, Zoltan Lukacs, Xiaoqi Ding, Michael Schulte-Markwort, Alfried Kohlschütter
JournalJournal of child neurology (J Child Neurol) Vol. 22 Issue 9 Pg. 1139-42 (Sep 2007) ISSN: 0883-0738 [Print] United States
PMID17890417 (Publication Type: Case Reports, Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Cerebroside-Sulfatase
Topics
  • Adolescent
  • Adult
  • Bone Marrow Transplantation (statistics & numerical data, trends)
  • Brain (metabolism, physiopathology)
  • Cerebroside-Sulfatase (metabolism)
  • Dementia (etiology, physiopathology)
  • Developmental Disabilities (etiology, physiopathology)
  • Disease Progression
  • Evoked Potentials, Auditory (physiology)
  • Female
  • Follow-Up Studies
  • Humans
  • Intellectual Disability (etiology, physiopathology)
  • Leukodystrophy, Metachromatic (metabolism, physiopathology, therapy)
  • Neural Conduction (physiology)
  • Paraplegia (etiology, physiopathology)
  • Peripheral Nerves (metabolism, physiopathology)
  • Time
  • Treatment Outcome

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: