Literature DB >> 26388597

X-linked adrenoleukodystrophy in a 6-year-old boy initially presenting with psychiatric symptoms.

Faruk İncecik1, M Özlem Hergüner, Gülen Mert, Neslihan Önenli-Mungan, Serdar Ceylaner, Deniz Kör, Şakir Altunbaşak.   

Abstract

X-linked adrenoleukodystrophy (ALD) leads to demyelination of the nervous system, adrenal insufficiency and accumulation of long-chain fatty acids. Most young patients with X-linked ALD develop seizures and progressive neurologic deficits, and die within the first two decades of life. We present the case of a 6-year-old with childhood-onset ALD, first presenting with psychiatric symptoms and progressive gait difficulties, slurred speech and cognitive impairment. Genetic testing was performed and a p.R401Q (c.1202G>A) mutation detected in the ABCD1 gene. ALD should be considered in the differential diagnosis of patients presenting with behavior changes and white matter disease in neuroimaging.

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Year:  2014        PMID: 26388597

Source DB:  PubMed          Journal:  Turk J Pediatr        ISSN: 0041-4301            Impact factor:   0.552


  1 in total

1.  X-linked Adrenoleukodystrophy in a 20-Year-Old Male With an ABCD1 Gene Mutation: First Case From Pakistan.

Authors:  Mariam Ghori; Rameen A Molani; Prof Mohsina N Ibrahim; Misbah I Hanif; Jamal Jamal Raza
Journal:  Cureus       Date:  2022-02-02
  1 in total

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