Condition
Bulbo-Spinal Atrophy, X-Linked
Neurology
Overview
An X-linked recessive form of spinal muscular atrophy. It is due to a mutation of the gene encoding the ANDROGEN RECEPTOR.
This information is general and should not be treated as medical advice. Always speak directly with a qualified healthcare professional before making decisions about treatment, diagnosis, procedures, medicines or care.
Quick facts about Bulbo-Spinal Atrophy, X-Linked
- Topic type
- Condition
- Category
- Neurology
- MeSH classification
- C10.228.854.468.399|C10.574.500.175|C10.574.562.500.374|C10.668.467.500.186|C16.320.322.076|C16.320.400.100
Preparing for an appointment about Bulbo-Spinal Atrophy, X-Linked
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- Ask what tests or assessments may be needed.
- Ask what treatment or management options may be suitable.
- Ask when you should seek urgent medical help or follow-up care.
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Source: Medical Subject Headings (MeSH), produced by the U.S. National Library of Medicine. EuroCareFinder is not endorsed by the National Library of Medicine. MeSH version: 2026.