X-vázaně recesivní
A slowly progressive motor neuronopathy caused by an expanded CAG repeat in the androgen receptor (AR) gene, with limb and bulbar weakness and mild androgen insensitivity.
Co se diagnózou změní
Physiotherapy, speech and swallowing assessment, endocrine follow-up, and genetic counselling for female relatives who may be carriers.
Analyzované geny
Známé také jako
Kennedy's disease; SBMA; SMAX1; spinal and bulbar muscular atrophy of Kennedy, X-linked recessive; spinal and bulbar muscular atrophy, X-linked 1; spinal and bulbar muscular atrophy, X-linked type 1; X-linked BSMA; X-linked bulbospinal amyotrophy; X-linked bulbospinal muscular atrophy; X-linked spinal and bulbar muscular atrophy
