Post 5-alpha-reductase inhibitors treatment syndrome
- Type
- Disease
- Group
- Disorder
- Inheritance
- Not applicable
- Status
- active
A rare neurologic disease characterized by persistent side effects of terminated 5-alpha-reductase inhibitor treatment, including impaired sexual function (low libido, erectile dysfunction, diminished semen volume and force), genital numbness or paresthesia, gynecomastia, depression, brain fog and elevated anxiety. Additional symptoms may include muscular problems (tics, muscle spasms, tremors, involuntary muscle contraction and muscular ache), joint pain, chronic fatigue, migraine, decreased body temperature and dry skin.
Names in Orphadata languages
9 of 12 languages| Lang | Name | Synonyms |
|---|---|---|
| en | Post 5-alpha-reductase inhibitors treatment syndrome | |
| fr | Syndrome post-traitement par inhibiteurs de la 5-alpha-reductase | |
| de | Post-5-alpha-Reduktase-Inhibitor-Syndrom | |
| es | Síndrome post-tratamiento con inhibidores de la 5-alfa-reductasa | |
| it | Sindrome post trattamento con gli inibitori della 5-alfa-reduttasi | |
| nl | Syndroom na behandeling met 5-alfa-reductaseremmers | |
| pt | Síndrome pós-tratamento com inibidores da 5-alfa-redutase | |
| pl | Post 5-alpha-reductase inhibitors treatment syndrome | |
| cs | Syndrom po léčbě inhibitory 5-alfa-reduktázy |
Definition in:
Cross-references
qualifier = Orphanet mapping relation| Source | Code | Qualifier | ICD relation | Validation |
|---|---|---|---|---|
| ICD-10 | F52.8 | NTBT | attributed | not yet validated |
| MONDO | 975897 | E | validated |
E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.
Classification
Preferential parent (Orphanet linearisation):
Parents in the classifications (1):
- ORPHA:98006Rare neurologic disease
rare neurological diseases
No children.
Genes
0 directOrphanet records no gene directly on this code.
Prevalence and incidence
0 recordsNo prevalence record in this release.
HPO phenotypes
Orphanet has no HPO annotation for this code in this release.
Sources for this card
- Orphanet page: orpha.net/en/disease/detail/686468
- This record as JSON: /data/d/686468.json