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Comparative Analysis of Cerebral Magnetic Resonance Imaging Changes in Nontreated Infantile, Juvenile and Adult Patients with Niemann-Pick Disease Type C.
Gburek-Augustat, Janina; Groeschel, Samuel; Kern, Jan; Beck-Woedl, Stefanie; Just, Jennifer; Harzer, Klaus; Stampfer, Miriam; Kraegeloh-Mann, Ingeborg.
Afiliação
  • Gburek-Augustat J; Division of Neuropaediatrics, Hospital for Children and Adolescents, University Leipzig, Leipzig, Germany.
  • Groeschel S; Department of Neuropaediatrics, Developmental Neurology, Social Paediatrics, University Children's Hospital Tuebingen, Tuebingen, Germany.
  • Kern J; Rare Disease Center Tuebingen, University of Tuebingen, Tuebingen, Germany.
  • Beck-Woedl S; Department of Neuropaediatrics, Developmental Neurology, Social Paediatrics, University Children's Hospital Tuebingen, Tuebingen, Germany.
  • Just J; Rare Disease Center Tuebingen, University of Tuebingen, Tuebingen, Germany.
  • Harzer K; Department of Neuropaediatrics, Developmental Neurology, Social Paediatrics, University Children's Hospital Tuebingen, Tuebingen, Germany.
  • Stampfer M; Rare Disease Center Tuebingen, University of Tuebingen, Tuebingen, Germany.
  • Kraegeloh-Mann I; Rare Disease Center Tuebingen, University of Tuebingen, Tuebingen, Germany.
Neuropediatrics ; 51(1): 37-44, 2020 02.
Article em En | MEDLINE | ID: mdl-31639880
ABSTRACT

AIM:

The study aims to describe cerebral MRI in different onset forms of Niemann-Pick type C (NPC). Systematic MRI analyses in this rare lysosomal storage disease are lacking in the infantile and juvenile onset forms.

METHODS:

Thirty-two cerebral MRI scans from 19 patients with NPC were assessed using a newly established and validated scoring system which addresses white matter changes and supratentorial versus infratentorial atrophy.

RESULTS:

Seven scans were from six NPC patients with early infantile onset (<2 years of age), six scans were from three patients with late infantile onset (2-6 years), six scans from four with juvenile onset (6-15 years), and 13 from six with adult onset (>15 years). While supratentorial atrophy was the leading sign in the infantile groups, the juvenile and adult forms were characterized by both, infra- and supratentorial atrophy. White matter changes were found in nearly every patient; they increased with the disease duration in the earlier forms and were prominent in the later forms already early in the disease course.

CONCLUSION:

This is the first systematic and comparative MRI analysis in the different onset groups of NPC using a scoring system. Early during disease course, MRI showed different patterns in infantile compared with juvenile and adult onset NPC patients, for example, only supratentorial atrophy in juvenile versus global atrophy in adult onset patients. MRI changes provide an additional, early biomarker for NPC.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Progressão da Doença / Doença de Niemann-Pick Tipo C / Substância Branca Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Progressão da Doença / Doença de Niemann-Pick Tipo C / Substância Branca Limite: Adolescent / Adult / Child / Child, preschool / Female / Humans / Male Idioma: En Ano de publicação: 2020 Tipo de documento: Article