Apologise, but: Dating a woman with muscular dystrophy
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Becker muscular dystrophy is an X-linked recessive inherited disorder characterized by slowly progressing wmoan weakness of the legs and pelvis. It is a type of dystrophinopathy. Becker muscular dystrophy is related to Duchenne muscular dystrophy in that both result from a mutation in the dystrophin gene, [4] but has a milder course. Individuals with this disorder typically experience progressive dating a woman with muscular dystrophy weakness of the leg and pelvis muscles, which is associated with a loss of muscle mass wasting. Muscle weakness also occurs in the arms, neck, and other areas, but not as noticeably severe as in the lower half of the body. Calf muscles initially enlarge during the ages of an attempt by the body to compensate for loss of wkman strengthbut the enlarged muscle tissue is eventually replaced by fat and connective tissue pseudohypertrophy as the legs become less used with use of wheelchair.
Possible complications associated with muscular dystrophies MD are cardiac arrhythmias.

The disorder is inherited with an X-linked recessive inheritance pattern. The gene is located on the X chromosome. Since women have two X chromosomes, if one X chromosome has the non-working gene, the second X chromosome will have a working copy of the gene to compensate, because of this ability to compensate, women rarely develop symptoms. All dystrophinopathies are inherited in an X-linked recessive manner.
Early Promise for Therapy Against Duchenne Muscular Dystrophy
The risk to the siblings of an affected individual depends upon the carrier status of the mother. Sons who inherit the mutation dating a woman with muscular dystrophy be affected; daughters who inherit the mutation will be carriers. Men who have Becker muscular dystrophy can have children, and all their daughters are carriers, but none of the sons will inherit their father's mutation. Becker muscular dystrophy occurs in approximately 1. Symptoms usually appear in men at about ages 8—25, but may sometimes begin later. Sons of a man with Becker muscular dystrophy do not develop the disorder, but daughters will be carriers and some carriers can womah some symptoms of muscular dystrophythe daughters' sons may develop the disorder.
In terms of the diagnosis of Becker muscular dystrophy symptom development resembles that dystropjy Duchenne muscular dystrophy. A physical exam indicates lack of pectoral and upper arm muscles, especially when the disease is unnoticed through the early teen years.
Dating A Woman With Muscular Dystrophy - 5 Reasons You Should Date A Single Mom | HuffPost Life
Muscle wasting begins in the legs and pelvis, then progresses to the muscles of the shoulders and neck. Calf muscle enlargement pseudohypertrophy is quite obvious. There is no known cure for Becker muscular dystrophy yet.

Treatment is aimed at control of symptoms to maximize the quality of life which can be measured by specific questionnaires. Inactivity such as bed rest or sitting down for too long can worsen the muscle disease. Physical therapy may be helpful to maintain muscle strength. Orthopedic appliances such as braces and wheelchairs may improve mobility and self-care.
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Immunosuppressant steroids have been known to help slow the progression of Becker muscular dystrophy. The cardiac problems that occur with EDMD and myotonic muscular dystrophy may require a pacemaker.

The investigational drug Debio is a known inhibitor of the protein cyclophilin D, which regulates the swelling of mitochondria in response to cellular injury. Upregulation of compensatory proteins has been done in models of transgenic mice.]
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