Home LiteratureArticle Details
PMID: 3386829 Published · ppublish English Case Reports Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity.

Neurology ·Vol. 38 ·No. 7 ·1988-07-00 ·Pages 1100-7

Naidu S, Hoefler G, Watkins PA, Chen WW, Moser AB, Hoefler S, Rance NE, Powers JM, Beard M, Green WR

Abstract

Neonatal hypotonia, seizures beginning at 5 days, and severe retardation were noted in a girl with normal karyotype and biochemical evidence of impaired adrenal function. Postmortem examination at 14 months revealed malformative and destructive lesions of central gray and white matter, atrophy of adrenal cortex with striated adrenocortical cells, hepatic fibrosis, and PAS-positive macrophages in several organs. Pathologically and clinically, this patient most closely approximated neonatal adrenoleukodystrophy (ALD) and differed strikingly from X-linked childhood ALD. In contrast, biochemical changes resembled the abnormalities observed in X-linked ALD and differed from those in the neonatal form. The very-long-chain fatty acid accumulation characteristic of both disorders was demonstrated, but unlike neonatal ALD, the levels or metabolism of plasmalogens, pipecolic acid, phytanic acid, and bile acid intermediates were normal, and peroxisomes in a liver biopsy specimen were present in normal number and appeared enlarged. While the case resembles the recently reported entity of peroxisomal acyl-CoA oxidase deficiency, assignment to this category was excluded by immunoblot studies on postmortem liver, which revealed normal amounts of this enzyme. Correlation of clinical, morphologic, and biochemical data suggests that this case is an example of a so-far undescribed entity, and reinforces the concept that the phenotypic spectrum of peroxisomal disorders is wider than realized.

MeSH Terms
Adrenoleukodystrophy/complications,genetics,physiopathology Catalase/metabolism Cells, Cultured Diffuse Cerebral Sclerosis of Schilder/genetics Fatty Acids/blood,metabolism Female Humans Infant, Newborn Intellectual Disability/complications,physiopathology Liver/metabolism,pathology,ultrastructure Microbodies/metabolism,ultrastructure Plasmalogens/biosynthesis Reference Values Seizures/complications,congenital,physiopathology Skin/metabolism X Chromosome
Chemicals
Fatty Acids Plasmalogens Catalase
Authors & Affiliations
10 authors, click to expand affiliations / ORCID
Naidu S
John F. Kennedy Institute, Baltimore, MD 21205.
Hoefler G
Watkins P A
Chen W W
Moser A B
Hoefler S
Rance N E
Powers J M
Beard M
Green W R
Article Info
Journal
Neurology
Abbr.
Neurology
ISSN
0028-3878
Published
1988-07-00
Pages
1100-7
Language
English
Region
United States
NLM ID
0401060
Subset
IM
Grants
NEI NIH HHS · EY 03168 · United States
NICHD NIH HHS · HD 10981 · United States
Analysis Services
Analysis Services

Contact

No. 2 Wenbo Road, Zhangqiu District, Jinan, Shandong

Qilu Normal University · Genelibs Bioinformatics Lab

750 Shunhua Rd, Jinan

2F, Bldg F, University Science Park

Tel: 0531-88819269

WeChat Official Account

Follow our WeChat subscription account for real-time updates and the latest in medical and biological research.


Business Email

E-mail: [email protected]