Medicine:Lyngstadaas syndrome
| Lyngstadaas syndrome | |
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| Other names | Steroid dehydrogenase deficiency-dental anomalies syndrome |
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| This condition is inherited in an autosomal recessive manner. | |
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 the Norwegian professor Ståle Petter Lyngstadaas.
Cause
Lyngstadaas syndrome is an autosomal recessive liver disease.[4]
Diagnosis
Management
Epidemiology
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. [citation needed]
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".[citation needed]
See also
References
- ↑ "Steroid dehydrogenase deficiency dental anomalies | Disease | Living With | Genetic and Rare Diseases Information Center (GARD) – an NCATS Program". https://rarediseases.info.nih.gov/gard/5015/steroid-dehydrogenase-deficiency-dental-anomalies/resources/3.
- ↑ Steroid dehydrogenase deficiency - dental anomalies Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.com
- ↑ RESERVED, INSERM US14 -- ALL RIGHTS. "Orphanet: Lyngstadaas syndrome". http://www.orpha.net/consor/cgi-bin/Disease_Search.php?lng=EN&data_id=1728&Disease_Disease_Search_diseaseType=ORPHA&Disease_Disease_Search_diseaseGroup=3196&Disease(s)/group%2520of%2520diseases=Lyngstadaas-syndrome&title=Lyngstadaas-syndrome&search=Disease_Search_Simple.
- ↑ RESERVED, INSERM US14-- ALL RIGHTS. "Orphanet: Steroid dehydrogenase deficiency dental anomalies syndrome" (in en). https://www.orpha.net/consor/cgi-bin/OC_Exp.php?lng=en&Expert=3196. Retrieved 26 September 2019.
External links
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| External resources |
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