Introduction/nouvelle

[Guest guest]

Hello, I present myself for the first time in your group. I am called

France and I am 30 years old. I was born by Caesarean and one

(doctors) called upon an anoxia néonatale without more precision. On

a more recent date,on invooqué a spino-cérébelleuse dégérescence more

precisely an ataxia of freidreich in 1988 but this one at summer

écartee by the genetics in May 2001 with the chu of Angers(france).On

also eliminated SCA1, SCA2, SCA3, SCA6 and SCA7.

In 2002 I consult Doctor andra Durr with the consultation of

genetics to the hopitale of Salpétrière Pity in Paris. Professor Durr

précisement assure me to a peripheric neuropathy a charcot-Marie-

tooht ,for the moment I am on standby to know the results of the

blood tests, which will determine the type of cmt.

I explain you now my history:

I have to start to walk at the 2 years age and half. To 6 years or 7

years I increased gutter plasters the night of it. Until worms the 10

years age I carried orthopedic shoes. At ten years one operates me

tendons on the left foot then at twelve years on the right foot. In

1990,je was operated one second time on the right foot, the

intervention rather worsened me. It arrives to me of the falls by

dérobements of the lower limbs but I them control better bus from

time to time I walk with canes English and then I have a feuteille

travelling handbook to rest .

In my family no case of cmt is known. My symptoms are a hypotonia, a

distal honest amiotrophie with the quatres members, a generalized

tendineuse aréflexie ostéo,un distal driving deficit. The feet are

cyanic and froids.La paralysis is abolished with the quatres members.

I hope to be able to discuss with you and to find the same symptoms

here.

Melle France BENOIT