Spastic Paraplegia Type 8

Also Known As:

Autosomal Dominant Spastic Paraplegia 8; Hereditary Spastic Paraplegia 8; Spastic Paraplegia 8; Spastic paraplegia 8, autosomal dominant; Spg 8

Networked: 2 relevant articles (0 outcomes, 0 trials/studies)

1.	Cicatrix (Scar)

Drugs and Important Biological Agents (IBA) related to Spastic Paraplegia Type 8:

1.	Wiskott-Aldrich Syndrome ProteinIBA 01/01/2018 - "The N471D and several other point mutations of human strumpellin (Str; also known as WASHC5), a member of the Wiskott-Aldrich syndrome protein and SCAR homologue (WASH) complex, have been shown to cause a form of HSP known as spastic paraplegia 8 (SPG8). "
2.	sarpogrelateIBA 01/01/2002 - "The patients were randomly allocated to two groups, including those receiving oral administration of 200 mg of sarpogrelate (SPG, 8 patients, age 61 +/- 6 years) and those receiving no medication (controls, 7 patients, age 57 +/- 8 years). "

1.	Oral Administration 01/01/2002 - "The patients were randomly allocated to two groups, including those receiving oral administration of 200 mg of sarpogrelate (SPG, 8 patients, age 61 +/- 6 years) and those receiving no medication (controls, 7 patients, age 57 +/- 8 years). "