Myotonic Dystrophy
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myotonic dystrophy , type 2: An inherited disorder of the ... ( cataracts ), cardiac abnormalities, ...
myotonic dystrophy (DM), also called dystrophia ... and females approximately equally. What is
myotonic dystrophy ? An example of an autosomal dominant ...
Stuttering
... no cure for stammering but many therapies can make a difference ...
myotonic dystrophy is due to a trinucleotide repeat (a " stuttering " sequence of three bases) in the DNA. The
myotonic dystrophy gene (called DM1), found on chromosome 19q13.3, codes for a ...
Galactose
... In most people the lactase enzyme levels decrease with age, so a person actually "grows into" lactose intolerance . These disorders include
myotonic dystrophy , the most common form of muscular dystrophy in adults, and galactose mia , a rare disorder that involves elevated levels of the sugar ...
Galactosemia
... , cephalo hematoma , polycythemia , G-6-P-D deficiency , and congenital rubella , syphilis , toxoplasmosis , ... These disorders include
myotonic dystrophy , the most common form of muscular dystrophy in adults, and galactosemia , a rare disorder that involves elevated levels of the sugar ...
Myotonia congenita
... However, many patients with myotonia do experience cramp ing from exercise . Symptoms of myotonia are often worse in the cold . Myotonias include
myotonic dystrophy , myotonia congenita , para myotonia congenita , and neuromyotonia. ...
Neurologic deficit
... s Muscle defects Connective tissue and skeletal defects Fetal crowding or fetal constraint Maternal neuromuscular disease s --
myotonic dystrophy and myasthenia gravis . Significant visual deficits are found in 10-50 percent of survivors, and other major neurologic deficit s in ...