Literature DB >> 36267868

Cribriform Appearance of White Matter in Canavan Disease Associated with Novel Mutations of ASPA Gene.

Maya Dattatraya Bhat1, Netravathi Manjunath2, Renu Kumari3, Mohammed Faruq4, Pramod Kumar Pal2, Chandrajit Prasad1, Ravindranadh Chowdary Mundlamuri2, Atchayaram Nalini2, Gautham Arunachal Udupi5, Priyanka Priyadarshini Baishya1, Karthik Kulanthaivelu1.   

Abstract

Cribriform appearance of the brain in Canavan disease is a rare finding. The two presented cases broaden the magnetic resonance imaging (MRI) phenotype wherein numerous oval, cystic structures, a few resembling dilated Virchow-Robin (VR) spaces, were noted in the centrum semiovale, periventricular, and lobar white matter producing a cribriform pattern. Besides, discrete round to oval cysts were present at the gray-white matter junctions in the second case, which were larger and appeared morphologically distinct from the VR spaces. These cysts did not elongate in any plane on imaging and were more representative of giant intramyelinic vacuoles. Genetic analysis revealed novel mutations in the aspartoacylase or ASPA gene that possibly accounts for the severe form of Canavan disease, which probably explains the imaging findings. The multicystic appearance of the white matter in Canavan disease is unusual and possibly represents two different histopathological substrates. Thieme. All rights reserved.

Entities:  

Keywords:  Canavan disease; cribriform; novel mutation

Year:  2021        PMID: 36267868      PMCID: PMC9578778          DOI: 10.1055/s-0041-1725118

Source DB:  PubMed          Journal:  J Pediatr Genet        ISSN: 2146-460X


  10 in total

1.  Spongy White Matter: A Novel Neuroimaging Finding in Canavan Disease.

Authors:  Mahesh Kamate; Vinayak Kabate; Mukul Malhotra
Journal:  Pediatr Neurol       Date:  2015-12-20       Impact factor: 3.372

Review 2.  Spongy degeneration of the brain, Canavan disease: biochemical and molecular findings.

Authors:  R M Matalon; K Michals-Matalon
Journal:  Front Biosci       Date:  2000-03-01

3.  Identification and expression of eight novel mutations among non-Jewish patients with Canavan disease.

Authors:  R Kaul; G P Gao; R Matalon; M Aloya; Q Su; M Jin; A B Johnson; R B Schutgens; J T Clarke
Journal:  Am J Hum Genet       Date:  1996-07       Impact factor: 11.025

4.  Leukodystrophy with multiple beaded periventricular cysts: unusual cranial MRI results in Canavan disease.

Authors:  Anne Drenckhahn; Markus Schuelke; Ellen Knierim
Journal:  J Inherit Metab Dis       Date:  2015-02-03       Impact factor: 4.982

5.  Teaching NeuroImages: honeycomb appearance of the brain in a patient with Canavan disease.

Authors:  Sunil Pradhan; Gourav Goyal
Journal:  Neurology       Date:  2011-03-29       Impact factor: 9.910

6.  Canavan disease: CT and MR imaging of the brain.

Authors:  J Brismar; G Brismar; G Gascon; P Ozand
Journal:  AJNR Am J Neuroradiol       Date:  1990 Jul-Aug       Impact factor: 3.825

7.  Aspartoacylase deficiency and N-acetylaspartic aciduria in patients with Canavan disease.

Authors:  R Matalon; K Michals; D Sebesta; M Deanching; P Gashkoff; J Casanova
Journal:  Am J Med Genet       Date:  1988-02

8.  The blood brain barrier in human leukodystrophies and allied diseases. Ultrastructural and morphometric studies on the capillaries in brain biopsies.

Authors:  A Kondo; K Suzuki
Journal:  Clin Neuropathol       Date:  1993 May-Jun       Impact factor: 1.368

9.  Magnetic resonance imaging in juvenile Canavan disease.

Authors:  P B Toft; R Geiss-Holtorff; M O Rolland; O Pryds; W Müller-Forell; E Christensen; W Lehnert; H C Lou; D Ott; J Hennig
Journal:  Eur J Pediatr       Date:  1993-09       Impact factor: 3.183

10.  The Clinical Features and Diagnosis of Canavan's Disease: A Case Series of Iranian Patients.

Authors:  Parvaneh Karimzadeh; Narjes Jafari; Habibe Nejad Biglari; Elham Rahimian; Farzad Ahmadabadi; Hamid Nemati; Mohamad Mehdi Nasehi; Mohammad Ghofrani; Mohsen Mollamohammadi
Journal:  Iran J Child Neurol       Date:  2014
  10 in total

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