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 1 - 10 of 333 for Congenital muscular dystrophy
  1. Fukuyama congenital muscular dystrophy 
    Fukuyama congenital muscular dystrophy is an inherited condition that predominantly affects the muscles, brain, and eyes. Congenital muscular dystrophies are ...
    https://medlineplus.gov/.../fukuyama-congenital-muscular-dystrophy - Genetics
  2. LMNA-related congenital muscular dystrophy 
    LMNA-related congenital muscular dystrophy (L-CMD) is a condition that primarily affects muscles used for movement (skeletal muscles). It is part of a group ...
    https://medlineplus.gov/...mna-related-congenital-muscular-dystrophy - Genetics
  3. Rigid spine muscular dystrophy 
    ... spine muscular dystrophy (RSMD) is a form of congenital muscular dystrophy. Disorders in this group cause muscle weakness and ... not show signs and symptoms of the condition. Congenital muscular dystrophy with spine rigidity syndrome Muscular dystrophy, congenital, merosin- ...
    https://medlineplus.gov/.../condition/rigid-spine-muscular-dystrophy - Genetics
  4. Collagen VI-related dystrophy 
    ... intermediate form is moderate in severity, and Ullrich congenital muscular dystrophy is the most severe.People with Bethlem muscular ... mechanical ventilation), particularly during sleep.People with Ullrich congenital muscular dystrophy have severe muscle weakness beginning soon after birth. ...
    https://medlineplus.gov/.../condition/collagen-vi-related-myopathy - Genetics
  5. FKTN gene 
    ... FKTN gene have been found to cause Fukuyama congenital muscular dystrophy, a condition that causes skeletal muscle weakness and brain and eye abnormalities. This form of congenital muscular dystrophy is seen almost exclusively in Japan. Virtually everyone ...
    https://medlineplus.gov/genetics/gene/fktn - Genetics
  6. Walker-Warburg syndrome 
    ... of a group of genetic conditions known as congenital muscular dystrophies, which cause muscle weakness and wasting (atrophy) beginning ... brain and eye anomalies], type A Walker-Warburg congenital muscular dystrophy Genetic Testing Registry: Walker-Warburg congenital muscular dystrophy ...
    https://medlineplus.gov/genetics/condition/walker-warburg-syndrome - Genetics
  7. Early-onset myopathy with fatal cardiomyopathy 
    ... symptoms of the condition. EOMFC Salih CMD Salih congenital muscular dystrophy Salih myopathy Titinopathy & early-onset myopathy with fatal ... A, Campbell KP. A novel form of familial congenital muscular dystrophy in two adolescents. Neuropediatrics. 1998 Dec;29(6): ...
    https://medlineplus.gov/...-onset-myopathy-with-fatal-cardiomyopathy - Genetics
  8. COL6A2 gene 
    ... VI 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
  9. COL6A1 gene 
    ... 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
  10. COL6A3 gene 
    ... VI 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
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · 8 · 9 · 10 · next