Your browser doesn't support javascript.
loading
Brainstem dominant form of X-linked adrenoleukodystrophy with a novel ABCD1 missense variant: A case report and literature review.
Kang, Yulai; Guo, Lu; Min, Zhuo; Zhang, Lei; Zhang, Lili; Tang, Chunhua.
Afiliación
  • Kang Y; Department of Neurology and Centre for Clinical Neuroscience, Daping Hospital, Army Medical Centre of PLA, Army Medical University, Chongqing, China.
  • Guo L; Department of Neurology and Centre for Clinical Neuroscience, Daping Hospital, Army Medical Centre of PLA, Army Medical University, Chongqing, China.
  • Min Z; Department of Neurology and Centre for Clinical Neuroscience, Daping Hospital, Army Medical Centre of PLA, Army Medical University, Chongqing, China.
  • Zhang L; Department of Neurology and Centre for Clinical Neuroscience, Daping Hospital, Army Medical Centre of PLA, Army Medical University, Chongqing, China.
  • Zhang L; Department of Neurology and Centre for Clinical Neuroscience, Daping Hospital, Army Medical Centre of PLA, Army Medical University, Chongqing, China.
  • Tang C; Department of Neurology and Centre for Clinical Neuroscience, Daping Hospital, Army Medical Centre of PLA, Army Medical University, Chongqing, China.
Mol Genet Genomic Med ; 12(7): e2499, 2024 Jul.
Article en En | MEDLINE | ID: mdl-39051462
ABSTRACT

BACKGROUND:

X-linked adrenoleukodystrophy (X-ALD) is the most common peroxisomal disorder attributed to ABCD1 mutations. Case reports with predominant brainstem involvement are rare. CASE PRESENTATION In this study, we reported a plateau male worker of X-ALD characterized by progressive weakness accompanied by gait instability, mild nystagmus, and constipation. After 2 years of onset, a brain Magnetic Resonance Image (MRI) scan showed no abnormality but genetic analysis revealed a heterozygous mutation (c.1534G>A) in the ABCD1 gene. After 7 years of onset, although the patient was given aggressive dietary and symptomatic treatment in the course of the disease, a brain MRI scan showed predominantly brainstem damage, but serum concentrations of very long-chain fatty acids were normal, and he had been bedridden for almost 2 years with severe bladder dysfunction, forcing him to undergo cystostomy. The patient was discharged with improved urinary retention and renal function.

CONCLUSIONS:

We reported an X-ALD patient with a novel ABCD1 variation characterized by brainstem damage and retrospectively summarized the clinical manifestation, MRI features, and genetic features of X-ALD patients with brainstem damage.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Asunto principal: Tronco Encefálico / Adrenoleucodistrofia / Mutación Missense / Miembro 1 de la Subfamilia D de Transportador de Casetes de Unión al ATP Límite: Adult / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Asunto principal: Tronco Encefálico / Adrenoleucodistrofia / Mutación Missense / Miembro 1 de la Subfamilia D de Transportador de Casetes de Unión al ATP Límite: Adult / Humans / Male Idioma: En Revista: Mol Genet Genomic Med Año: 2024 Tipo del documento: Article País de afiliación: China