Annals of Indian Academy of Neurology
CASE REPORT
Year
: 2014  |  Volume : 17  |  Issue : 3  |  Page : 361--363

Adrenomyeloneuropathy with bulbar palsy: A rare association


Vishal Annaji Chafale, Satish Arunkumar Lahoti, Atanu Biswas, Arijit Roy, Asit Kumar Senapati 
 Department of Neurology, Bangur Institute of Neurosciences, Kolkata, West Bengal, India

Correspondence Address:
Atanu Biswas
Department of Neurology, Bangur Institute of Neurosciences, 52/1A, S. N. Pandit Street, Kolkata - 700 025, West Bengal
India

Adrenomyeloneuropathy (AMN) is a variant of adrenoleukodystrophy (ALD), an X-linked recessive peroxisomal disorder associated with accumulation of very long chain fatty acids (VLCFA). Mutations of this gene lead to abnormal peroxisomal β-oxidation, which results in the harmful accumulation of VLCFAs in affected cells. Neurological symptoms occur due to progressive demyelination and destruction of cerebral white matter and primary adrenal insufficiency. Bulbar palsy in a case of AMN is very unusual. We report a case of a 22-year-old male with AMN who developed adrenal insufficiency at the age of 4 years successfully treated by gluco- and mineralocorticoids followed by features of myeloneuropathy with bulbar palsy. AMN with prominent bulbar symptoms emphasizes the diverse clinical manifestation of this disease.


How to cite this article:
Chafale VA, Lahoti SA, Biswas A, Roy A, Senapati AK. Adrenomyeloneuropathy with bulbar palsy: A rare association.Ann Indian Acad Neurol 2014;17:361-363


How to cite this URL:
Chafale VA, Lahoti SA, Biswas A, Roy A, Senapati AK. Adrenomyeloneuropathy with bulbar palsy: A rare association. Ann Indian Acad Neurol [serial online] 2014 [cited 2021 Jan 18 ];17:361-363
Available from: https://www.annalsofian.org/article.asp?issn=0972-2327;year=2014;volume=17;issue=3;spage=361;epage=363;aulast=Chafale;type=0