Literature DB >> 11315202

MRI and proton spectroscopy in Lowe syndrome.

J F Schneider1, E Boltshauser, T J Neuhaus, C Rauscher, E Martin.   

Abstract

The oculocerebrorenal syndrome of Lowe (OCRL) is an X-linked disorder characterized by major abnormalities of eyes, nervous system, and kidneys. We report two patients with typical intracranial lesions on MRI. The proton spectroscopy study of the periventricular white matter showed a moderate elevation of the signal at 3.56 ppm in the patient with cystic lesions. This resonance is usually assigned to myo-inositol and interpreted as a glial marker. In our patient it could also represent a true accumulation inside the cysts of phosphatidylinositol 4,5-biphosphate which is not degraded in patients with Lowe syndrome.

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Year:  2001        PMID: 11315202     DOI: 10.1055/s-2001-12221

Source DB:  PubMed          Journal:  Neuropediatrics        ISSN: 0174-304X            Impact factor:   1.947


  6 in total

1.  Incomplete cryptic splicing by an intronic mutation of OCRL in patients with partial phenotypes of Lowe syndrome.

Authors:  Eiji Nakano; Amine Yoshida; Yudai Miyama; Tomoo Yabuuchi; Yuko Kajiho; Shoichiro Kanda; Kenichiro Miura; Akira Oka; Yutaka Harita
Journal:  J Hum Genet       Date:  2020-05-19       Impact factor: 3.172

Review 2.  MR spectroscopy in children: protocols and pitfalls in non-tumorous brain pathology.

Authors:  Jacques F Schneider
Journal:  Pediatr Radiol       Date:  2016-05-27

Review 3.  Pediatric neurodegenerative white matter processes: leukodystrophies and beyond.

Authors:  Jonathan A Phelan; Lisa H Lowe; Charles M Glasier
Journal:  Pediatr Radiol       Date:  2008-04-30

4.  Locus heterogeneity of Dent's disease: OCRL1 and TMEM27 genes in patients with no CLCN5 mutations.

Authors:  Enrica Tosetto; Maria Addis; Gianluca Caridi; Cristiana Meloni; Francesco Emma; Gianluca Vergine; Gilda Stringini; Teresa Papalia; Giancarlo Barbano; Gian Marco Ghiggeri; Laura Ruggeri; Nunzia Miglietti; Angela D Angelo; Maria Antonietta Melis; Franca Anglani
Journal:  Pediatr Nephrol       Date:  2009-07-07       Impact factor: 3.714

5.  Interaction of Rab31 and OCRL-1 in oligodendrocytes: its role in transport of mannose 6-phosphate receptors.

Authors:  A G Rodriguez-Gabin; E Ortiz; K Demoliner; Q Si; G Almazan; J N Larocca
Journal:  J Neurosci Res       Date:  2010-02-15       Impact factor: 4.164

6.  Splicing Analysis of Exonic OCRL Mutations Causing Lowe Syndrome or Dent-2 Disease.

Authors:  Lorena Suarez-Artiles; Ana Perdomo-Ramirez; Elena Ramos-Trujillo; Felix Claverie-Martin
Journal:  Genes (Basel)       Date:  2018-01-04       Impact factor: 4.096

  6 in total

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