Motor Development and Orthoses in Spinal Muscular Atrophy (SMA)

Azienda USL Reggio Emilia - IRCCS

Status: Completed

Conditions: Spinal Muscular Atrophy

Study type: Observational

Funder types: Other

Identifiers

NCT00961103

UDGEE-SMA

Details and patient eligibility

About

Spinal Muscular Atrophy (SMA) is neurodegenerative disease of anterior horn cells of spinal cord and represents the second more frequent pathology in childhood.

According to the age of onset and the maximum motor function the disorder is classified in 4 types. Patients with SMA II and SMA III often use orthoses to achieve postural and dynamic functions.

In this retrospective observational study the investigators describe the characteristics of sitting position, standing and walking correlated to type and time of orthoses used.

Full description

We collect data from patients with SMA II and SMA III referred to UDGEE from jan. 1995 to dec. 2008.

We estimate to achieve informations about 50-70 patients.

Enrollment: 80 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Clinical and genetics diagnosis of SMA II and SMA III

Exclusion criteria

• N/A

Trial design

80 participants in 1 patient group

SMA II and SMA III

Description:

patients with SMA II and SMA III