TNP03-related limb-girdle muscular dystrophy D2

Get in touch with RARE Concierge.

Contact RARE Concierge

Synonyms: Autosomal dominant limb-girdle muscular dystrophy type 1F | LGMD type 1F | LGMD1F | Limb-girdle muscular dystrophy type 1F

A rare subtype of autosomal dominant limb-girdle muscular dystrophy with a variable age of onset characterized by progressive proximal weakness and wasting of the shoulder and pelvic musculature (with the pelvic girdle and especially the ileopsoas muscle being more affected) and frequent association of calf hypertrophy dysphagia arachnodactyly with or without finger contractures and/or distal and axial muscle involvement. Additional features include an abnormal gait exercise intolerance myalgia fatigue and respiratory insufficiency. Cardiac conduction defects are typically not observed.

Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview. Reference: Access aggregated data from Orphanet at Orphadata. Orphadata: Free access data from Orphanet. © INSERM 1999. Available on Data version June 2024

Newly diagnosed with
TNP03-related limb-girdle muscular dystrophy D2?

Our RARE Concierge Services Guides are available to assist you by providing information, resources and connections as you navigate your rare disease journey.

Get Concierge Help

Advocacy Organizations

Don't see your organization here. Let us know here.

Clinical Trials

For a list of clinical trials in this disease area, please click here.