Maternally inherited Leigh syndrome.

Details

Serval ID
serval:BIB_23CFAEDF4EBE
Type
Article: article from journal or magazin.
Publication sub-type
Case report (case report): feedback on an observation with a short commentary.
Collection
Publications
Institution
Title
Maternally inherited Leigh syndrome.
Journal
Journal of Pediatrics
Author(s)
Ciafaloni E., Santorelli F.M., Shanske S., Deonna T., Roulet E., Janzer C., Pescia G., DiMauro S.
ISSN
0022-3476
Publication state
Published
Issued date
1993
Peer-reviewed
Oui
Volume
122
Number
3
Pages
419-422
Language
english
Notes
Publication types: Case Reports ; Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, P.H.S.
Abstract
A 6 1/2-year-old girl had developmental regression, and Leigh syndrome was diagnosed. A second girl born to the same mother after heterologous artificial insemination also lost acquired skills and died at 2 1/2 years of age; neuropathologic examination confirmed the diagnosis of Leigh syndrome. Tissues from both children and from the mother had a point mutation at nucleotide 8993 in the adenosinetriphosphatase 6-gene of mitochondrial DNA. This family illustrates that Leigh syndrome can be transmitted by maternal inheritance.
Keywords
Adenosine Triphosphatases/genetics, Child, DNA, Mitochondrial/genetics, Female, Humans, Leigh Disease/genetics, Point Mutation/genetics, Polymerase Chain Reaction, Polymorphism, Restriction Fragment Length
Pubmed
Web of science
Create date
12/01/2010 10:04
Last modification date
20/08/2019 14:01
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