Brain magnetic resonance imaging findings in patients with mucopolysaccharidosis VI. Issue 2 (21st November 2012)
- Record Type:
- Journal Article
- Title:
- Brain magnetic resonance imaging findings in patients with mucopolysaccharidosis VI. Issue 2 (21st November 2012)
- Main Title:
- Brain magnetic resonance imaging findings in patients with mucopolysaccharidosis VI
- Authors:
- Azevedo, Ana C. M.
Artigalás, Osvaldo
Vedolin, Leonardo
Komlós, Márcia
Pires, Adriana
Giugliani, Roberto
Schwartz, Ida Vanessa D. - Abstract:
- Abstract: Introduction: Mucopolysaccharidosis type VI (MPS VI) is a rare lysosomal storage disorder caused by the deficient activity of N‐ acetylgalactosamine 4‐sulfatase. MPS VI is usually considered as not being associated with mental retardation. Aims/methods: The main objective of the present study was to describe brain magnetic resonance imaging (MRI) findings and their correlation with clinical and biochemical findings in MPS VI patients. The study was conducted at Hospital de Clínicas de Porto Alegre, Brazil with 25 MPS VI patients. All patients were evaluated through clinical evaluation, IQ tests, urinary glycosaminoglycans (GAG) analysis, and brain MRI. Results: Mean age at evaluation was 10.6 ± 4.52 years. Five of 16 patients presented total IQ below the normal range. Brain MRI was abnormal in the majority of patients ( n = 19/21), and the most frequent abnormalities found were the presence of dilated perivascular spaces and white matter lesions. Correlations were found between age and normalized white matter lesion load (NLL) ( r = 0.46; p = 0.04) and normalized cerebral volume (NCV) ( r = −0.56; p = 0.01), between NLL and height deficit ( r = 0.48; p = 0.04), and between NCV and weight deficit ( r = −0.58; p = 0.01) and height deficit ( r = −0.55; p = 0.01). A correlation between urinary GAG levels and quantitative brain MRI findings was not found, neither between qualitative and quantitative brain MRI findings and IQ scores. Conclusions: MPS VIAbstract: Introduction: Mucopolysaccharidosis type VI (MPS VI) is a rare lysosomal storage disorder caused by the deficient activity of N‐ acetylgalactosamine 4‐sulfatase. MPS VI is usually considered as not being associated with mental retardation. Aims/methods: The main objective of the present study was to describe brain magnetic resonance imaging (MRI) findings and their correlation with clinical and biochemical findings in MPS VI patients. The study was conducted at Hospital de Clínicas de Porto Alegre, Brazil with 25 MPS VI patients. All patients were evaluated through clinical evaluation, IQ tests, urinary glycosaminoglycans (GAG) analysis, and brain MRI. Results: Mean age at evaluation was 10.6 ± 4.52 years. Five of 16 patients presented total IQ below the normal range. Brain MRI was abnormal in the majority of patients ( n = 19/21), and the most frequent abnormalities found were the presence of dilated perivascular spaces and white matter lesions. Correlations were found between age and normalized white matter lesion load (NLL) ( r = 0.46; p = 0.04) and normalized cerebral volume (NCV) ( r = −0.56; p = 0.01), between NLL and height deficit ( r = 0.48; p = 0.04), and between NCV and weight deficit ( r = −0.58; p = 0.01) and height deficit ( r = −0.55; p = 0.01). A correlation between urinary GAG levels and quantitative brain MRI findings was not found, neither between qualitative and quantitative brain MRI findings and IQ scores. Conclusions: MPS VI patients may present abnormal IQ scores without correlation with brain abnormalities on the MRI, a finding which was found to be very frequent in MPS VI. Additional studies are required to confirm our findings. … (more)
- Is Part Of:
- Journal of inherited metabolic disease. Volume 36:Issue 2(2013)
- Journal:
- Journal of inherited metabolic disease
- Issue:
- Volume 36:Issue 2(2013)
- Issue Display:
- Volume 36, Issue 2 (2013)
- Year:
- 2013
- Volume:
- 36
- Issue:
- 2
- Issue Sort Value:
- 2013-0036-0002-0000
- Page Start:
- 357
- Page End:
- 362
- Publication Date:
- 2012-11-21
- Subjects:
- Metabolism, Inborn errors of -- Periodicals
Metabolism -- Disorders -- Periodicals
616.39042 - Journal URLs:
- http://www.springer.com/gb/ ↗
- DOI:
- 10.1007/s10545-012-9559-x ↗
- Languages:
- English
- ISSNs:
- 0141-8955
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5006.950000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10206.xml