Content area

|
|

Genetisk rådgivning er relevant både ved familiære og sporadiske tilfælde af amyotrofisk lateral sklerose

Forfatter(e)
Suzanne Granhøj Lindquist1, 2, Morten Dunø1, Kirsten Svenstrup2 & Jørgen Erik Nielsen2 1) Klinisk Genetisk Klinik, Rigshospitalet 2) Hukommelsesklinikken, Rigshospitalet Ugeskr Læger 2014;176:V01140023
Reference: 
Ugeskr Læger 2014;176:V01140023
Blad nummer: 
Sidetal: 
2457-2460
Genetic counselling is relevant in familial as well as sporadic cases of amyotrophic lateral sclerosis
Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disease of upper and lower motor neurons which often results in death from respiratory failure within 2-4 years. It has been estimated that 5-10% of ALS patients have a family history with ALS. The genetic background of the disorder is heterogeneous, and recently molecular genetic testing has become increasingly relevant, also in the clinical evaluation. As several genes have been identified in which the pathogenic mutations are characterized by reduced age-dependent penetrance, genetic testing can be relevant to consider, also in isolated cases.
Du skal være logget ind for at læse denne artikel
Log ind

Right side

af Marianne Carisius Kastrup | 06/12
2 kommentarer
af Mats Lindberg | 06/12
1 Kommentar
af Jens Ole Mathiesen | 06/12
2 kommentarer
af Jørn Bøgh | 06/12
2 kommentarer
af Anna Inger Roe Rasmussen | 02/12
18 kommentarer
af Troels Krogh Nielsen | 30/11
7 kommentarer
af Flemming Juul Hansen | 29/11
1 Kommentar