Phenotype, Genotype & Biomarkers in ALS and Related Disorders

The goals of this study are: (1) to better understand the relationship between the phenotype
and genotype of amyotrophic lateral sclerosis (ALS) and related diseases, including primary
lateral sclerosis (PLS), hereditary spastic paraplegia (HSP), progressive muscular atrophy
(PMA), and frontotemporal dementia (FTD); and (2) to develop biomarkers that might be useful
in aiding therapy development for this group of disorders.

Eligibility Criteria

Inclusion Criteria:

- Member of at least one of the following categories:

1. Individuals with a clinical diagnosis of ALS or a related disorder, including
FTD, HSP, PLS, PMA and MSP (sporadic or familial).

2. Family member of an enrolled affected individual.

- Able and willing to comply with relevant procedures.

Exclusion Criteria:

- Affected with end or late stage disease.

- A condition or situation which, in the PI's opinion, could confound the study finding
or may interfere significantly with the individual's participation and compliance
with the study protocol. This includes (but is not limited to) neurological,
psychological and/or medical conditions.

Principal Investigator

Richard Barohn, MD

Study Contact

Yolanda Harness 913-945-9928, yharness@kumc.edu

Estimated Completion Date

Thursday, August 1, 2019

ClinicalTrials.gov #

NCT02327845
05/19/2015