Maternally inherited Leigh syndrome.


Autoria(s): Ciafaloni E.; Santorelli F.M.; Shanske S.; Deonna T.; Roulet E.; Janzer C.; Pescia G.; DiMauro S.
Data(s)

1993

Resumo

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.

Identificador

http://serval.unil.ch/?id=serval:BIB_23CFAEDF4EBE

isbn:0022-3476

pmid:8095070

doi:10.1016/S0022-3476(05)83431-6

isiid:A1993KQ59200017

Idioma(s)

en

Fonte

Journal of Pediatrics, vol. 122, no. 3, pp. 419-422

Palavras-Chave #Adenosine Triphosphatases/genetics; Child; DNA, Mitochondrial/genetics; Female; Humans; Leigh Disease/genetics; Point Mutation/genetics; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length
Tipo

info:eu-repo/semantics/article

article