Literature DB >> 20185470

Adult peroxisomal acyl-coenzyme A oxidase deficiency with cerebellar and brainstem atrophy.

Sacha Ferdinandusse1, Simon Barker, Katherine Lachlan, Marinus Duran, Hans R Waterham, Ronald J A Wanders, Simon Hammans.   

Abstract

Peroxisomal acyl-coenzyme A oxidase deficiency (formerly also called pseudoneonatal adrenoleucodystrophy) is a disorder of peroxisomal fatty acid oxidation with a severe presentation. Most patients present at birth or in early infancy, and the mean age of death was 5 years in a recently published cohort of 22 patients. Brain imaging shows a progressive leucodystrophy. The authors report here the first adult patients (two siblings, 52 and 55 years old) with peroxisomal acyl-coenzyme A oxidase deficiency with a remarkably mild clinical presentation. Magnetic resonance brain imaging revealed profound atrophy of the brainstem and cerebellum.

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Year:  2010        PMID: 20185470     DOI: 10.1136/jnnp.2009.176255

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  7 in total

1.  Effects of hematopoietic stem cell transplantation on acyl-CoA oxidase deficiency: a sibling comparison study.

Authors:  Raymond Y Wang; Edwin S Monuki; James Powers; Phillip H Schwartz; Paul A Watkins; Yang Shi; Ann Moser; David A Shrier; Hans R Waterham; Diane J Nugent; Jose E Abdenur
Journal:  J Inherit Metab Dis       Date:  2014-03-12       Impact factor: 4.982

Review 2.  Fatty Acid Oxidation in Peroxisomes: Enzymology, Metabolic Crosstalk with Other Organelles and Peroxisomal Disorders.

Authors:  Ronald J A Wanders; Frédéric M Vaz; Hans R Waterham; Sacha Ferdinandusse
Journal:  Adv Exp Med Biol       Date:  2020       Impact factor: 2.622

3.  Pseudo-neonatal Adrenoleukodystrophy: A Rare Peroxisomal Disorder.

Authors:  Cheshta Arora; Hansashree Padmanabha; Rita Christopher; Rohan Mahale; Maya Bhat; Gautham Arunachal; Ravi Shekhar; Pooja Mailankody; P S Mathuranath
Journal:  Ann Indian Acad Neurol       Date:  2021-10-11       Impact factor: 1.714

4.  Adult-onset cerebello-brainstem dominant form of X-linked adrenoleukodystrophy presenting as multiple system atrophy: case report and literature review.

Authors:  Kotaro Ogaki; Shunsuke Koga; Naoya Aoki; Wenlang Lin; Kinuko Suzuki; Owen A Ross; Dennis W Dickson
Journal:  Neuropathology       Date:  2015-07-31       Impact factor: 1.906

Review 5.  Peroxisomes in brain development and function.

Authors:  Johannes Berger; Fabian Dorninger; Sonja Forss-Petter; Markus Kunze
Journal:  Biochim Biophys Acta       Date:  2015-12-11

6.  Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency.

Authors:  Hugh J McMillan; Thea Worthylake; Jeremy Schwartzentruber; Chloe C Gottlieb; Sarah E Lawrence; Alex Mackenzie; Chandree L Beaulieu; Petra A W Mooyer; Ronald J A Wanders; Jacek Majewski; Dennis E Bulman; Michael T Geraghty; Sacha Ferdinandusse; Kym M Boycott
Journal:  Orphanet J Rare Dis       Date:  2012-11-22       Impact factor: 4.123

7.  Whole Exome Sequencing Reveals Compound Heterozygosity for Ethnically Distinct PEX7 Mutations Responsible for Rhizomelic Chondrodysplasia Punctata, Type 1.

Authors:  Jessie C Jacobsen; Emma Glamuzina; Juliet Taylor; Brendan Swan; Shona Handisides; Callum Wilson; Michael Fietz; Tessa van Dijk; Bart Appelhof; Rosamund Hill; Rosemary Marks; Donald R Love; Stephen P Robertson; Russell G Snell; Klaus Lehnert
Journal:  Case Rep Genet       Date:  2015-10-26
  7 in total

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