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MRI and (1)H-MRS in adenosine kinase deficiency.
Staufner, C; Blom, H J; Dionisi-Vici, C; Freisinger, P; Makhseed, N; Ballhausen, D; Kölker, S; Hoffmann, G F; Harting, I.
Afiliación
  • Staufner C; Department of General Pediatrics, Division of Neuropediatrics and Pediatric Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Blom HJ; Center for Pediatrics and Adolescent Medicine, University Hospital Freiburg, Freiburg, Germany.
  • Dionisi-Vici C; Division of Metabolism, Bambino Gesù Children's Hospital IRCCS, Rome, Italy.
  • Freisinger P; Children's Hospital Reutlingen, Reutlingen, Germany.
  • Makhseed N; Department of Pediatrics, Jahra Hospital, Jahra, Kuwait.
  • Ballhausen D; Center for Molecular Diseases, CHUV Lausanne, Lausanne, Switzerland.
  • Kölker S; Department of General Pediatrics, Division of Neuropediatrics and Pediatric Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Hoffmann GF; Department of General Pediatrics, Division of Neuropediatrics and Pediatric Metabolic Medicine, University Hospital Heidelberg, Heidelberg, Germany.
  • Harting I; Department of Neuroradiology, University Hospital Heidelberg, Im Neuenheimer Feld 400, 69120, Heidelberg, Germany. inga.harting@med.uni-heidelberg.de.
Neuroradiology ; 58(7): 697-703, 2016 Jul.
Article en En | MEDLINE | ID: mdl-26993811
ABSTRACT

INTRODUCTION:

Adenosine kinase deficiency (ADK deficiency) is a recently described disorder of methionine and adenosine metabolism resulting in a neurological phenotype with developmental delay, muscular hypotonia, and epilepsy as well as variable systemic manifestations. The underlying neuropathology is poorly understood. We have investigated MRI and (1)H-MRS changes in ADK deficiency in order to better understand the in vivo neuropathologic changes of ADK deficiency.

METHODS:

Systematic evaluation of 21 MRIs from eight patients (age range 9 days-14.6 years, mean 3.9 years, median 2.7 years) including diffusion-weighted imaging in six and (1)H-MRS in five patients.

RESULTS:

Brain maturation was delayed in the neonatal period and in infancy (6/6), but ultimately complete. White matter changes occurring in five of eight patients were discrete, periventricular, and unspecific (4/5), or diffuse with sparing of optic radiation, corona radiata, and pyramidal tracts (1/5). Choline was low in white matter spectra (3/3), while there was no indication of low creatine in white matter or basal ganglia (5/5), and diffusion was variably decreased or increased. Central tegmental tract hyperintensity was a common finding (6/8), as was supratentorial atrophy (6/8).

CONCLUSIONS:

MRI changes in ADK deficiency consist of delayed but ultimately completed brain maturation with later onset of mostly unspecific white matter changes and potentially transient central tegmental tract hyperintensity. Immaturity on neonatal MRI is consistent with prenatal onset of disease and reduced choline with lower membrane turnover resulting in delayed myelination and deficient myelin maintenance.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encéfalo / Encefalopatías Metabólicas / Imagen por Resonancia Magnética / Adenosina Quinasa / Espectroscopía de Protones por Resonancia Magnética Tipo de estudio: Diagnostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Neuroradiology Año: 2016 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Encéfalo / Encefalopatías Metabólicas / Imagen por Resonancia Magnética / Adenosina Quinasa / Espectroscopía de Protones por Resonancia Magnética Tipo de estudio: Diagnostic_studies Límite: Adolescent / Child / Child, preschool / Female / Humans / Infant / Male / Newborn Idioma: En Revista: Neuroradiology Año: 2016 Tipo del documento: Article País de afiliación: Alemania
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