A look at life with Muscular Dystrophy

When it comes to living with Becker’s Muscular Dystrophy from time to time I wake up in the morning and right away I know it’s going to .

21 Truths People With Muscular Dystrophy Wish Others Understood

21 Truths People With Muscular Dystrophy Wish Others Understood

Muscular Dystrophy is often confused with Multiple Sclerosis when they are completely separate from each other. Here is a great pin to share to help raise awareness and learn the difference between the two. #musculardystrophy #MultipleSclerosis please visit www.my-beckers-story.blogspot.com

Muscular Dystrophy is often confused with Multiple Sclerosis when they are completely separate from each other.

Myotonic Dystrophy and the Brain - Myotonic Dystrophy Support Group

Myotonic Dystrophy and the Brain Dr Richard Petty, Neurologist, Glasgow Brain involvement …

Vitamin D deficiency in myotonic dystrophy type 1. - PubMed - NCBI

Vitamin D deficiency in myotonic dystrophy type 1. - PubMed - NCBI

6 Self-Care Tips for Living With Myotonic Dystrophy

6 Self-Care Tips for Living With Myotonic Dystrophy

Learn self-care tips for living with myotonic dystrophy, a rare, genetic condition.

Best practice guidelines and recommendations on the molecular diagnosis of myotonic dystrophy types 1 and 2

Myotonic dystrophy is an autosomal dominant, multisystem disorder that is characterized by myotonic myopathy. The symptoms and severity of myotonic dystrophy type l ranges from severe and congenital forms, which frequently result in death because .

Myotonic Dystrophy - symptoms, Definition, Description, Demographics, Causes and symptoms, Diagnosis, Treatment

Myotonic Dystrophy - symptoms, Definition, Description, Demographics, Causes and symptoms, Diagnosis, Treatment

6 Self-Care Tips for Living With Myotonic Dystrophy

6 Self-Care Tips for Living With Myotonic Dystrophy

Learn self-care tips for living with myotonic dystrophy, a rare, genetic condition.

fibromyalgia symptoms | Fibromyalgia (FM) Tragic Misdiagnosis – Myotonic Dystrophy Type 2 ...

Fibromyalgia (FM) Tragic Misdiagnosis – Myotonic Dystrophy Type 2 and Cervical Spinal Stenosis – New Treatments as Result

22q11.2 deletion syndrome, which has several presentations including DiGeorge syndrome (DGS), DiGeorge anomaly,[2][3] velo-cardio-facial syndrome, Shprintzen syndrome, conotruncal anomaly face syndrome, Strong syndrome, congenital thymic aplasia, and thymic hypoplasia is a syndrome caused by the deletion of a small piece of chromosome 22.

Bethlem myopathy is an autosomal dominant myopathy, classified as a congenital form of muscular dystrophy, that is caused by a mutation in one of three genes .

Pinterest
Search