z-logo
open-access-imgOpen Access
Infantile Alexander disease: A rare leukodystrophy
Author(s) -
K. Jagadish Kumar,
Harish Kumar Suryaprakash,
V. G. Manjunath,
S Harsha
Publication year - 2012
Publication title -
journal of pediatric neurosciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.247
H-Index - 18
eISSN - 1998-3948
pISSN - 1817-1745
DOI - 10.4103/1817-1745.102573
Subject(s) - macrocephaly , leukodystrophy , medicine , krabbe disease , magnetic resonance imaging , disease , pediatrics , pathology , radiology
Infantile Alexander disease (AD) is a rare leukodystrophy characterized by its early onset within 2 years of life and clinically presents with macrocephaly, seizures, and retarded psychomotor development. Magnetic resonance imaging (MRI) shows characteristic symmetric white matter abnormalities with frontal predominance. We present a case of infantile AD with typical clinical characteristics and MRI features.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here