Nutrition Health Chat: Tuesday, Dec. 8th, 5-6 PM Eastern. Learn how vitamins, minerals, and phytonutrients affect your health. Free live Q&A. Join us!
Member Comments are provided by individuals and reflect their personal opinions only. Under NO circumstances should you act on any advice or opinion posted in this forum.  ALWAYS check with your personal physician before taking any action regarding your health! MedHelp International and our partners, sponsors and affiliates have no obligation to monitor any comments posted on this site, or the content and/or accuracy of such exchanges. MedHelp International does not endorse the views of any user.
Neurology  (Expert Forum)
 | 
Re: DNA test for limb girdle disease
This forum is for questions and support regarding neurology issues such as: Alzheimer's Disease, ALS, Autism, Brain Cancer, Cerebral Palsy, Chronic Pain, Epilepsy, Fibromyalgia, Headaches, MS, Neuralgia, Neuropathy, Parkinson's Disease, RSD, Sleep Disorders, Stroke, Traumatic Brain Injury.

Re: DNA test for limb girdle disease

by CCF Neuro[P] MD RPS, Jan 01, 1995 12:00AM
Posted By CCF Neuro[P] MD, RPS on January 25, 1999 at 08:42:36:

In Reply to: DNA test for limb girdle disease posted by MDB on January 23, 1999 at 16:33:39:






My doctor sent me to the local hospital to get a dna test for limb girdle disease and for center cores disease the head of the lab was sure these test existed but was unaware as to wwho might do them.
My question is there such test ? If so do you know a place that does them?
Thanks,
MDB
Dear MDB:
Sorry to hear about your health problems.  As far as I know, there is no definite DNA test for limb girdle disease.  The usual concern is differentiating from Becker's.  There is a DNA test for Becker's, and this can be sent to Boston Universtiy, Center for Human Genetics.  The problem is that we think Limb-girdle musclualr dystrophy is not a single entity, and at least eight different genetic defects have been identified.  There is a autosomal dominant and recessive type of Limb-girdle.  The defects have been found on chromosome 1,5 for the autosomal dominant type, and chomosomees 2, 4, 5,13, 15, and 17 for the autosomal recessive type.  Furthermore there are two types that the chromsomal defect has not been found.  A muscle biopsy, lab findings, and clinical findings are the usual way to diagnose this entity.  Center core disease, although some forms are associated with a ion channel defect, as far as I am aware there is not commerical DNA test available.  Again, the muscle biopsy, basic lab values, and
clinical exam are the current means of diagnosis.  Sorry, I can be of better help with the information you wanted.
Sincerely,
CCF Neuro[P] MD, RPS  
Continue discussion
RSS Expert Activity
In the ER: Coffee, anyone?
4 hrs ago by Jon Geller, D.V.M.
My animal blogs! 
6 hrs ago by Justine Lee, D.V.M., DACVECC
Prevention Gains Momentum: Your Gui... 
Nov 29 by Lee Kirksey, MD