Lyngstadaas syndrome
From Infogalactic: the planetary knowledge core
| Lyngstadaas syndrome | |
|---|---|
| Classification and external resources | |
| Specialty | Lua error in Module:Wikidata at line 446: attempt to index field 'wikibase' (a nil value). |
| Patient UK | Lyngstadaas syndrome |
| MeSH | C537490 |
Lyngstadaas Syndrome, also known as severe dental aberrations in familial steroid dehydrogenase deficiency [1], is a rare autosomal recessive liver disease involving an enzyme (steroid dehydrogenase) deficiency and dental anomalies.[2][3] The disease is named after Professor Ståle Petter Lyngstadaas.
Demographics
Office of Rare Diseases listed Lyngstadaas syndrome as a "rare disease". This means that Lyngstadaas syndrome, or a subtype of Lyngstadaas syndrome, affects less than 200,000 people in the US population.
Orphanet, a consortium of European partners, currently defines a condition rare when if affects 1 person per 2,000. They list Lyngstadaas syndrome as a "rare disease".
See also
References
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
- ↑ Steroid dehydrogenase deficiency - dental anomalies Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.com
- ↑ Lua error in package.lua at line 80: module 'strict' not found.
