A PHP Error was encountered

Severity: Warning

Message: file_get_contents(https://...@pubfacts.com&api_key=b8daa3ad693db53b1410957c26c9a51b4908&a=1): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests

Filename: helpers/my_audit_helper.php

Line Number: 176

Backtrace:

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 176
Function: file_get_contents

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 250
Function: simplexml_load_file_from_url

File: /var/www/html/application/helpers/my_audit_helper.php
Line: 3122
Function: getPubMedXML

File: /var/www/html/application/controllers/Detail.php
Line: 575
Function: pubMedSearch_Global

File: /var/www/html/application/controllers/Detail.php
Line: 489
Function: pubMedGetRelatedKeyword

File: /var/www/html/index.php
Line: 316
Function: require_once

Adult Krabbe Disease That Was Successfully Treated with Intravenous Immunoglobulin. | LitMetric

AI Article Synopsis

  • Krabbe disease is caused by a deficiency of the galactocerebrosidase enzyme, leading to harmful metabolite buildup and nerve damage, causing symptoms like spastic paraplegia.
  • A 14-year-old girl with symptoms resembling Guillain-Barré syndrome was treated with intravenous immunoglobulin (IVIg), resulting in improvement of her limb weakness.
  • Further tests at age 16 indicated adult Krabbe disease, suggesting that IVIg might be a promising treatment option for managing symptoms of this condition.

Article Abstract

Krabbe disease involves the accumulation of neurotoxic metabolites due to lysosomal galactocerebrosidase enzyme deficiency, which results in widespread demyelination of central and peripheral nerves. Generally, Krabbe disease presents as spastic paraplegia with a slow progressive course; however, some cases may show clinical symptoms similar to those of chronic inflammatory demyelinating polyneuropathy (CIDP). No previously reported studies have investigated the efficacy of intravenous immunoglobulin (IVIg) for treating Krabbe disease, and reporting a case involving IVIg treatment may be informative in the clinical setting. A 14-year-old girl who developed Guillain-Barré syndrome-like limb weakness was administered IVIg, and her limb weakness improved. At 16 years old, she developed abnormal sensory perception and weakness of both upper limbs. A nerve conduction study revealed demyelination, which led us to suspect CIDP. IVIg was administered, and her symptoms gradually improved. A nerve biopsy, enzyme activity, and genetic test results indicated adult Krabbe disease. In some cases, IVIg may be an effective treatment for Krabbe disease.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8112994PMC
http://dx.doi.org/10.2169/internalmedicine.6094-20DOI Listing

Publication Analysis

Top Keywords

krabbe disease
24
adult krabbe
8
intravenous immunoglobulin
8
limb weakness
8
disease
6
krabbe
5
ivig
5
disease treated
4
treated intravenous
4
immunoglobulin krabbe
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!