The following information is available on wikipedia - and if this truly is a genetic issue, MMS will not help it, because MMS works on pathogens, inflammation, etc.
This article is about a type of spinal muscular atrophy linked to a genetic defect in the AR gene. For a list of other conditions with similar names, see Spinal muscular atrophies.
Spinal and bulbar muscular atrophy
Classification and external resources
ICD-10 G12.1
ICD-9 335.1
OMIM 313200
DiseasesDB 7144
eMedicine article/1172604
MeSH D055534
Spinal and bulbar muscular atrophy (SBMA), also known as spinobulbar muscular atrophy, bulbo-spinal atrophy, X-linked bulbospinal neuropathy (XBSN), X-linked spinal muscular atrophy type 1 (SMAX1), and Kennedy's disease (KD) — is a debilitating neurodegenerative disease resulting in muscle cramps and progressive weakness due to degeneration of motor neurons in the brain stem and spinal cord.
The condition is associated with mutation of the androgen receptor (AR) gene[1][2][3] and is inherited in a X-linked recessive manner. As with many genetic disorders, no cure is known, although research continues.
Because of its endocrine manifestations related to the impairment of the AR gene, SMBA can be viewed as a variation of the disorders of the androgen insensitivity syndrome (AIS). It is also related to other neurodegenerative diseases caused by similar mutations, such as Huntington's disease and the spinocerebellar ataxias.
