Doctor insights on:
What Is Cone Dystrophy
Problem withcolor ey: The most common symptoms of cone dystrophy are vision loss (age of onset ranging from the late teens to the sixties), sensitivity to bright lights, and poor color vision. Therefore, patients see better at dusk. Visual acuity usually deteriorates gradually, but it can deteriorate rapidly to 20/200; later, in more severe cases, it drops to counting fingers vision. ...Read moreSee 1 more doctor answer
Inherited disorder: Dystrophies are inherited disorders. For the cornea, there are many dystrophies. The most common corneal dystrophy is the anterior basement membrane corneal dystrophy. It is also called map-dot-fingerprint dystrophy. ...Read more
Corneal lining: The inner lining of the cornea consists of cells which pump fluid from the cornea keeping it clear. When these cells are deficient or incompetent, the cornea swells with fluid. This when spontaneous is called fuch's. Surgical replacement of the cells from a donor can restore clarity in a procedure called dsek. ...Read more
Muscle disease: Muscular dystrophy is a worsening disorder that causes muscle weakness. The worst kind is duchenne's dystrophy, that affects only boys, leads to severe weakness, and wheelchair needs, breathing difficulties in the teens. Milder forms can present later or not cause as much disability. These are genetic (runs in families) disorders. ...Read moreSee 1 more doctor answer
Cone Biopsy: A cone biopsy is a larger form of a cervical biopsy that often removes a cone-shaped piece of tissue from the cervix. Many times it removes tissue that is high in the cervical canal as well as tissue that is on the surface of the cervix. It will often include tissue that your health practitioner thinks is abnormal. ...Read more
Symptomatic Therapy: Myotonic dystrophy is probably the most common form of muscular dystrophy. It is a multisystem disease that includes dystrophy of muscle, myotonia, cardiopathy, ocular cataracts, and endocrinopathy. Myotonia can be treated with anticonvulsant drugs, cardiac , ocular and endocrine symptoms are treated as they would be in any other patient. There is no specific therapy for the underlying disorder. ...Read more
Big biopsy of cervix: While the patient is under anesthesia (asleep) the doctor cuts out a small (outside) cone shaped portion of the cervix that has abnormal/ pre cancerous or cancerous skin and deeper tissue . It can treat cervical dysplasia ( pre cancer of the cervix) or diagnose cervical cancer. It is rarely enough to treat cervical cancer. ...Read moreSee 1 more doctor answer
Macula: Macula is the central part of the retina that does the fine focus. Maculopathy is when there is a disease process causing damage to macula. That can be from drugs, diabetes, .... Macular dystrophy can be confusing. Macula is a type of spot. So if it is used in relation to cornea, that is a separate issue. In terms of retina... A disease process that is genetically predestined. ...Read moreSee 1 more doctor answer
Need data: Is it primary or secondary fsgs. In addition how much protein is in the urine and what is the current kidney function? If the kidney function is significantly depressed the prognosis is poor. If there is more than 4000mg protein in the urine the prognosis is poor. Primary fsgs has a worse prognosis than secondary fsgs. Follow up with a nephrologist for appropriate treatment. ...Read more
Childhood: This is a class of hereditary disorders affecting the white matter of the brain mainly presenting in childhood. The diseases may vary in extent and pace, but often affect walking, cognition, and may be associated with epilepsy. More information may be found on mayo clinic site or www.Aan.Com. ...Read more
Muscle disorder: Muscular dystrophy includes a number of disorders which are associated primarily with abnormalities of the architecture of the cells, often causing changes in size and function (weakness). These disorders are typically inherited, and recognized early in life, although there are of course exceptions to this. Prognosis is based on the type of MD and expression of the specific geneotype. ...Read more
Inborn muscle diseas: Nih website has lots of excellent information: http://www.Ninds.Nih.Gov/disorders/md/md.Htm "the muscular dystrophies (md) are a group of more than 30 genetic diseases characterized by progressive weakness and degeneration of the skeletal muscles that control movement. Some forms of md are seen in infancy or childhood, while others may not appear until middle age or later. ". ...Read more
See this site : http://www.parentprojectmd.org/site/pageserver?pagename=care_stage_adult.Get a more detailed answer ›
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