|
Andrew M. Ball, MS, PT -> Re: Fibromyalgia in an 8 y.o. boy (January 17, 2001 5:42:00 AM)
|
Betty,
I'd be doubtful that an 8 year old boy actually has fibroM. It's usually found in women, and has been linked to sleeping disorders. Furthermore, the pain would be more diffuse and systemic than you describe. FibroM is often a trash diagnosis used when the PCP can't find any other cause for the pain (kind of like the old ortho diagnosis of IDK, which either stood for internally deranged knee . . . or I don't know).
But I digress . . .
Even if a connective tissue disorder has been clinically "ruled out," I'd be concerned that something may have been missed. Unless the child had a muscle biopsy (which is typically avoided if at all possible) or a genetic evaluation to search for the marker (specifically at Xp21) you can't be sure.
The mere fact that the child's younger brothers are beginning to present in a similar manner is cause enough for concern. This is begining to sound suggestive of Duchenne Muscular Dystrophy (DMD). DMD usually shows up at about 5 years of age + or - 3 years, though Becker syndrome (a less severe form of DMD), tends to be less severe and has a later onset (e.g. it can also show up at about age 8).
To start with, I'd suggest evaluating from that perspective. Look for a Gower sign when the child gets to standing from the floor (e.g. walking up the legs with his hands), and pseudohypoertrophy of the calf, triceps and gluteal muscles. In many cases, they will feel thick and rubbery to palpation.
Good luck and let us know what develops!
Andrew M. Ball, MS, MBA, PT
[This message has been edited by Andrew M. Ball, MS, PT (edited January 17, 2001).]
|
|
|
|