Question:
What are many chances of getting ALS if my dad or mom had it?
ALS familiar
ALS familiar se hereda en un patrón genético dominante. Esta forma de esclerosis lateral amiotrófica es visto sólo en cinco a 10 por ciento de los casos de ELA. Una mutación del gen de la superóxido dismutasa (SOD1) en el cromosoma 21 se encontró que la causa de la ELA familiar en 20 por ciento de estos pacientes, sin embargo la causa en el 80 por ciento restante se desconoce.
Dado que la mutación genética se hereda en un patrón autosómico dominante, la descendencia de una persona con ELA familiar tendrá una probabilidad del 50 por ciento de ser diagnosticados con esta enfermedad.
ALS Frequently Asked Questions
Has there been a lot of research completed on ALS?
My doctor has prescribed Rilutek. How does this drug function?
Has the ALS Association funded any research?
Can you provide more details about TREAT ALS?
Should I consider participating in ALS Research?
How does Phase III clinical research trials differ from Phase I and Phase II?
Which centers are working on ALS research?
Has research been previously completed on ALS?
Are there any upcoming trials to look forward to?
Help me find information on ALS Research?
Which diseases are the differential diagnosis for ALS?
I have been feeling weaknes in my body. Could it be ALS?
I have been referred to a neurologist. What can I expect during this visit?
How important is the neurological exam in diagnosing ALS?
Which laboratory tests are necessary to diagnose ALS?
I am scheduled for a CSF analysis. What does this test mean?
Why did the neurologist schedule an MRI for me?
I have heard an Electromyography is important in diagnosing ALS. Can you explain it a little more?
I wonder if bone cancer is causing my symptoms?
Are there more than one form of ALS?
Tell me more about Sporadic ALS? How common is it?
What are many chances of getting ALS if my dad or mom had it?
Is Guamanian ALS only located in Guam?
How do the different forms of ALS differ?
Who first made wrote details on ALS?
What are the incidence and prevalence rates of ALS?
Is ALS known as any other names?
What is Amyotrophic Lateral Sclerosis (ALS)?
What symptoms can I expect during the early stages of this disease?
I developed muscle weakness and was later diagnosed with ALS. Is it commmon to feel this weak?
What symptoms can I expect with upper motor neuron involvement?
What symptoms can I expect with lower motor neuron involvement?
Can I expect any other symptoms as I battle ALS?
Which symptoms am I not likely to experience with ALS?
What is the difference between Limb-onset ALS versus Bulbar-onset ALS?
"Spastic bulbar palsy" sounds complicated. What is it exactly?
What can I expect during the end stages of ALS?
Is Rilutek the only medication used in ALS?
Will I benefit from physical therapy as an ALS patient?
Is occupational therapy necessary when diagnosed with ALS?
I am noticing problems with my speech. Can a speech pathologist help me?
My father who has ALS has stopped eating large meals. What do I do?
I have just been diagnosed with ALS and need to talk to someone. Who do I talk to?
I have heard I will develop problems with breathing. Which type of doctor do I see?
What is the purpose of the ALS C.A.R.E. database?
