Literature DB >> 23430902

Neurodegeneration with Brain Iron Accumulation on MRI: An Adult Case of α-Mannosidosis.

Evelien Zoons1, Tom J de Koning, Nico G G M Abeling, Marina A J Tijssen.   

Abstract

CASE: A 34-year-old woman was referred to our hospital with progressive movement disorders and neurodegeneration with brain iron accumulation and enlargement of the frontal diploe on the MRI. Metabolic testing revealed that she had α-mannosidosis (AMD), a lysosomal storage disorder.
BACKGROUND: AMD is a rare genetic disorder that causes α-mannosidase deficiency resulting in lysosomal accumulation of undigested oligosaccharides. The symptoms of AMD consist of facial and skeletal deformities combined with progressive psychiatric and neurological complaints, especially ataxia and mental retardation. Bilateral patellar dislocation and hearing impairment are frequent. DISCUSSION: The movement disorders we found in our patient have not been reported previously, but they are likely late symptoms of this progressive disorder. The iron deposits in the basal ganglia have also not been reported in AMD and are yet of unknown significance. Lysosomal storage disorders, such as AMD, should be considered in patients with progressive neurologic conditions and neurodegeneration with brain iron accumulation on MRI.

Entities:  

Year:  2011        PMID: 23430902      PMCID: PMC3509898          DOI: 10.1007/8904_2011_78

Source DB:  PubMed          Journal:  JIMD Rep        ISSN: 2192-8304


  11 in total

1.  MRI of mannosidosis.

Authors:  M Patlas; M Y Shapira; A Nagler; R Sheffer; J M Gomori
Journal:  Neuroradiology       Date:  2001-11       Impact factor: 2.804

2.  Adult alpha-mannosidosis: clinical progression in the absence of demyelination.

Authors:  A Gutschalk; I Harting; M Cantz; C Springer; K Rohrschneider; H-M Meinck
Journal:  Neurology       Date:  2004-11-09       Impact factor: 9.910

3.  Neurology of adult alpha-mannosidosis.

Authors:  S Niemann; M Beck; G Seidel; J Spranger; P Vieregge
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-07       Impact factor: 10.154

Review 4.  Molecular genetic approaches to understanding the roles and regulation of iron in brain health and disease.

Authors:  Daniel Johnstone; Elizabeth A Milward
Journal:  J Neurochem       Date:  2010-03-24       Impact factor: 5.372

5.  Mannosidosis: a clinical and histopathologic study.

Authors:  B Kjellman; I Gamstorp; A Brun; P A Ockerman; B Palmgren
Journal:  J Pediatr       Date:  1969-09       Impact factor: 4.406

Review 6.  Decreased T2 signal in the thalami may be a sign of lysosomal storage disease.

Authors:  Taina Autti; Raimo Joensuu; Laura Aberg
Journal:  Neuroradiology       Date:  2007-03-03       Impact factor: 2.804

Review 7.  Clinical and genetic delineation of neurodegeneration with brain iron accumulation.

Authors:  A Gregory; B J Polster; S J Hayflick
Journal:  J Med Genet       Date:  2008-11-03       Impact factor: 6.318

8.  Mannosidosis: pathology of the nervous system.

Authors:  J H Sung; M Hayano; R J Desnick
Journal:  J Neuropathol Exp Neurol       Date:  1977 Sep-Oct       Impact factor: 3.685

9.  MR findings in mannosidosis.

Authors:  J L Dietemann; M M Filippi de la Palavesa; C Tranchant; B Kastler
Journal:  Neuroradiology       Date:  1990       Impact factor: 2.804

Review 10.  Alpha-mannosidosis.

Authors:  Dag Malm; Øivind Nilssen
Journal:  Orphanet J Rare Dis       Date:  2008-07-23       Impact factor: 4.123

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  5 in total

1.  Coexisting variants in OSTM1 and MANEAL cause a complex neurodegenerative disorder with NBIA-like brain abnormalities.

Authors:  Diran Herebian; Bader Alhaddad; Annette Seibt; Thomas Schwarzmayr; Katharina Danhauser; Dirk Klee; Stefani Harmsen; Thomas Meitinger; Tim M Strom; Ansgar Schulz; Ertan Mayatepek; Tobias B Haack; Felix Distelmaier
Journal:  Eur J Hum Genet       Date:  2017-06-14       Impact factor: 4.246

Review 2.  Cerebral Iron Deposition in Neurodegeneration.

Authors:  Petr Dusek; Tim Hofer; Jan Alexander; Per M Roos; Jan O Aaseth
Journal:  Biomolecules       Date:  2022-05-17

Review 3.  In Vivo NMR Studies of the Brain with Hereditary or Acquired Metabolic Disorders.

Authors:  Erica B Sherry; Phil Lee; In-Young Choi
Journal:  Neurochem Res       Date:  2015-11-26       Impact factor: 3.996

4.  Disentangling in vivo the effects of iron content and atrophy on the ageing human brain.

Authors:  S Lorio; A Lutti; F Kherif; A Ruef; J Dukart; R Chowdhury; R S Frackowiak; J Ashburner; G Helms; N Weiskopf; B Draganski
Journal:  Neuroimage       Date:  2014-09-28       Impact factor: 6.556

5.  Mutations, Genes, and Phenotypes Related to Movement Disorders and Ataxias.

Authors:  Dolores Martínez-Rubio; Isabel Hinarejos; Paula Sancho; Nerea Gorría-Redondo; Raquel Bernadó-Fonz; Cristina Tello; Clara Marco-Marín; Itxaso Martí-Carrera; María Jesús Martínez-González; Ainhoa García-Ribes; Raquel Baviera-Muñoz; Isabel Sastre-Bataller; Irene Martínez-Torres; Anna Duat-Rodríguez; Patrícia Janeiro; Esther Moreno; Leticia Pías-Peleteiro; Mar O'Callaghan Gordo; Ángeles Ruiz-Gómez; Esteban Muñoz; Maria Josep Martí; Ana Sánchez-Monteagudo; Candela Fuster; Amparo Andrés-Bordería; Roser Maria Pons; Silvia Jesús-Maestre; Pablo Mir; Vincenzo Lupo; Belén Pérez-Dueñas; Alejandra Darling; Sergio Aguilera-Albesa; Carmen Espinós
Journal:  Int J Mol Sci       Date:  2022-10-06       Impact factor: 6.208

  5 in total

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