Maternally inherited Leigh syndrome.
| 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 |