Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 11 - 20 of 68 for Progressive muscular dystrophy
  1. Walker-Warburg syndrome 
    ... a group of genetic conditions known as congenital muscular dystrophies, which cause muscle weakness and wasting (atrophy) beginning ... signs and symptoms of the condition. Cerebroocular dysplasia-muscular dystrophy syndrome Chemke syndrome COD-MD syndrome HARD syndrome ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  2. Collagen VI-related dystrophy 
    ... VI-related dystrophy, which range in severity: Bethlem muscular dystrophy is the mildest, an intermediate form is moderate in severity, and Ullrich congenital muscular dystrophy is the most severe.People with Bethlem muscular ...
    https://medlineplus.gov/.../condition/collagen-vi-related-myopathy - Genetics
  3. POMT1 gene 
    ... of a group of disorders known as congenital muscular dystrophies. Individuals with Walker-Warburg syndrome have skeletal muscle ... Condition MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/pomt1 - Genetics
  4. POMT2 gene 
    ... of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes muscle weakness and abnormalities ... Condition MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy More About This Health Condition Mutations in the ...
    https://medlineplus.gov/genetics/gene/pomt2 - Genetics
  5. CRPPA gene 
    ... of a group of disorders known as congenital muscular dystrophies. Walker-Warburg syndrome causes skeletal muscle weakness and ... Condition MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy More About This Health Condition 2-C-methyl- ...
    https://medlineplus.gov/genetics/gene/crppa - Genetics
  6. COL6A1 gene 
    ... Condition MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy More About This Health Condition alpha 1 (VI) ... mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2005 Jan 15;14(2): ...
    https://medlineplus.gov/genetics/gene/col6a1 - Genetics
  7. COL6A2 gene 
    ... Condition MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy More About This Health Condition CO6A2_HUMAN collagen ... mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2005 Jan 15;14(2): ...
    https://medlineplus.gov/genetics/gene/col6a2 - Genetics
  8. COL6A3 gene 
    ... Condition MedlinePlus Genetics provides information about Limb-girdle muscular dystrophy More About This Health Condition CO6A3_HUMAN collagen ... mutations are a common cause of Ullrich congenital muscular dystrophy. Hum Mol Genet. 2005 Jan 15;14(2): ...
    https://medlineplus.gov/genetics/gene/col6a3 - Genetics
  9. DMD gene 
    ... people with the Duchenne and Becker forms of muscular dystrophy. These conditions occur almost exclusively in males and ... nucleotides) in the gene.Mutations that cause Becker muscular dystrophy, which typically has milder features and appears at ...
    https://medlineplus.gov/genetics/gene/dmd - Genetics
  10. DYSF gene 
    ... the DYSF gene that can cause limb-girdle muscular dystrophy type 2B have been identified. Limb-girdle muscular dystrophy is a group of related disorders characterized by ...
    https://medlineplus.gov/genetics/gene/dysf - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next