Arbre Généalogique Guertin Rondeau Family Tree - Person Sheet
Arbre Généalogique Guertin Rondeau Family Tree - Person Sheet
NameNicolas Fache 
Birthabt 1643, Saint-Éloi De Meneslies, Amiens, Picardie, France2
Death3 Dec 1714, Charlesbourg, Québec, Canada2
Burial4 Dec 1714, Saint-Charles-Borromée, Charlesbourg, Québec, Canada2
FatherJean Fache
MotherMarie Granserre
Spouses
Birthabt 1651, Saint-Sulpice, Saint-Germain-Des-Prés, Paris, France2
Death30 Oct 1728, Charlesbourg, Québec, Canada2
Burial31 Oct 1728, Saint-Charles-Borromée, Charlesbourg, Québec, Canada2
FlagsDNA Disorder, Fille du Roi
FatherJean Suret
MotherDenise Leconfesseur
Marriage7 Oct 1669, Notre-Dame-De-Québec, Québec, Canada2
ChildrenClaudine (1685-1742)
Notes for Catherine (Spouse 1)
2Fille du Roi, arrivée en 16693
13Disorders with distinctive features in French Canadians includes,
"Lebers hereditary optic neuropathy "This optic disease causes acute or subacute central vision loss, followed by optic atrophy. It is associated with three major mutations in the mitochondrial DNA (mtDNA). Haplotype analysis suggests that most French Canadians with this disease descend from one founder, fille du roi Catherine Suret, with the mutation T14484C. This mutation accounts for 86% of all French-Canadian cases of Lebers. Dutch victims with the same mutation share the same haplotype with the French-Canadian victims, suggesting a possible common origin of this mutation prior to 1600. Lebers primarily strikes young adu lt males (only one in four victims is female). In some cases vision eventually improves, but most remain legally blind."
posted May 16, 2016 by [Living Lambert]
13Disorders with distinctive features in French Canadians includes,
"Lebers hereditary optic neuropathy "This optic disease causes acute or subacute central vision loss, followed by optic atrophy. It is associated with three major mutations in the mitochondrial DNA (mtDNA). Haplotype analysis suggests that most French Canadians with this disease descend from one founder, fille du roi Catherine Suret, with the mutation T14484C. This mutation accounts for 86% of all French-Canadian cases of Lebers. Dutch victims with the same mutation share the same haplotype with the French-Canadian victims, suggesting a possible common origin of this mutation prior to 1600. Lebers primarily strikes young adu lt males (only one in four victims is female). In some cases vision eventually improves, but most remain legally blind."
posted May 16, 2016 by [Living Lambert]
Notes for Nicolas & Catherine (Family)
Ménage établi a Charlesbourg, 10 enfants de cette union3