Idiopathic disease
An idiopathic disease is any disease with an unknown cause or mechanism of apparent spontaneous origin.[1]
For some medical conditions, one or more causes are somewhat understood, but in a certain percentage of people with the condition, the cause may not be readily apparent or characterized. In these cases, the origin of the condition is said to be idiopathic. With some other medical conditions, the root cause for a large percentage of all cases has not been established—for example,
Derivation
The term 'idiopathic' derives from Greek ἴδιος idios "one's own" and πάθος pathos "suffering", idiopathy means approximately "a disease of its own kind".
Examples
Diseases where the cause is seen as wholly or partly idiopathic include:
- Idiopathic pulmonary fibrosis
- Idiopathic pulmonary haemosiderosis
- Idiopathic intracranial hypertension
- Idiopathic chronic fatigue
- Granulomatous prostatitis
Medical advances and this term
Advances in medical science improve the understanding of causes of diseases and the classification of diseases; thus, regarding any particular condition or disease, as more root causes are discovered and as events that seemed spontaneous have their origins revealed, the percentage of cases designated as idiopathic decreases.
Usage of synonyms
The word essential is sometimes synonymous with idiopathic (as in essential hypertension, essential thrombocythemia, and essential tremor) and the same is true of primary (as in primary biliary cholangitis, or primary amenorrhea), with the latter term being used in such cases to contrast with secondary in the sense of "secondary to [i.e., caused by] some other condition." Another, less common synonym is agnogenic (agno-, "unknown" + -gen, "cause" + -ic).
The word cryptogenic ( The use of cryptogenic is also sometimes reserved for cases where it is presumed that the cause is simple and will be found in the future.
Some congenital conditions are idiopathic, and sometimes the word congenital is used synonymously with idiopathic; but careful usage prefers to reserve the word congenital for conditions to which the literal sense of the word applies (that is, those whose pathophysiology has existed since the neonatal period).
Syndrome without a name
The term syndrome without a name (SWAN) is used "when a child or young adult is believed to have a genetic condition and testing has failed to identify its genetic cause". It is believed that "about half (50%) of children with learning disabilities and approximately 60% of children with congenital disabilities (disabilities which are apparent from birth) do not have a definitive diagnosis to explain the cause of their difficulties".[6][7]
See also
- Diagnosis of exclusion
- Embolic stroke of undetermined source
- Functional disorder
- Idiosyncratic drug reaction
- Fever of unknown origin
References
- ISBN 9780199557141. Retrieved 2014-01-18.
- S2CID 11321176.
- ^ a b "Frequently Asked Questions About Epilepsy | CDC". www.cdc.gov. 26 October 2022. Retrieved 1 April 2023.
- ^ PMID 29590333.
- ^ "cryptogenic". Dorland's Illustrated Medical Dictionary. Elsevier.
- ^ "What does SWAN or being undiagnosed mean?". Genetic Alliance UK. 22 March 2017. Retrieved 16 April 2019.
- ^ "Syndromes without a name (SWAN)". Raising Children Network (Australia). 10 January 2017. Retrieved 16 April 2019.
External links
The dictionary definition of idiopathic disease at Wiktionary
