Clinical and Functional Assessment of Patients With Inherited Non-Duchenne Myopathies in Sohag University Hospital

Plain-language summary

This observational study aims to evaluate the clinical and functional features of children with inherited non-Duchenne myopathies (a group of inherited muscle disorders causing muscle weakness). Patients aged 2-18 with a diagnosis confirmed by clinical, laboratory, and genetic testing can take part. It is a study without an assigned phase and is still enrolling participants.

The summary above is a plain-language rendering of the official record. The original English title is shown for reference.

Trial details

Phase

N/A

Status

Recruiting

Sponsor

Sohag University

Start date

8/1/2024

Estimated completion

8/1/2025

Countries

Egypt

Related genes

Locations

• Sohag, Egypt
• Sohag, Egypt
• Sohag, Egypt

Eligibility criteria

Criteria are reproduced from the ClinicalTrials.gov record in the original English. Only the trial team can determine eligibility.

Inclusion Criteria:

* • Age between 2 and 18 years

  * Confirmed diagnosis of non-DMD based on clinical features, laboratory investigations, and genetic testing.
  * Patients and their parents agree to participate in the study.

Exclusion Criteria:

* • Children with a confirmed diagnosis of DMD

  * Children with incomplete medical records or unavailable clinical data.
  * Children with endocrinal ,nutritional critical care and inflammatory myopathies.
  * Other neuromuscular disorders that affect AHC or nerves as SMA, congenital myasthenia Gravis and neuropathic.
  * Other acquired neuromuscular disorders as Guillain Barre syndrome and toxic myopathy.
  * Patients and their parents refuse to participate in the study.