Results for dystrofia myotonica

dystrofia myotonica

Myotonic Dystrophy Type 1 GeneReviews NCBI Bookshelf.
For a description of databases Locus Specific, HGMD, ClinVar to which links are provided, click here. OMIM Entries for Myotonic Dystrophy Type 1 View All in OMIM. View in own window. MYOTONIC DYSTROPHY 1; DM1. DYSTROPHIA MYOTONICA PROTEIN KINASE; DMPK.
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Myotonic Dystrophy Type 2 GeneReviews NCBI Bookshelf.
Myotonic dystrophy type 2 DM2 is characterized by myotonia 90% of affected individuals and muscle dysfunction weakness, pain, and stiffness 82%, and less commonly by cardiac conduction defects, iridescent posterior subcapsular cataracts, insulin-insensitive type 2 diabetes mellitus, and testicular failure.
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Dystrofia myotonika type 1 gode råd YouTube.
Published on Jun 28, 2016. Helene Knutsen og Solveig Skåla har diagnosen dystrofia myotonika type 1. I dette intervjuet gir de gode råd til personer som får diagnosen og dere som jobber med personer med diagnosen. Standard YouTube License. Show more Show less.
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Myotonic dystrophy Wikipedia.
Synonyms Dystrophia myotonica, 1 myotonia atrophica, 1 myotonia dystrophica 1. 40-year-old with myotonic dystrophy who presented with muscle wasting, bilateral cataracts, and complete heart block. Specialty Medical genetics, pediatrics. Symptoms Muscle loss, weakness, muscles which contract and are unable to relax 1.

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