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Lyngstadaas syndrome
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Lyngstadaas syndrome : ウィキペディア英語版
Lyngstadaas syndrome

Lyngstadaas Syndrome (named after Professor Ståle Petter Lyngstadaas) is a rare liver disease involving an enzyme (steroid dehydrogenase) deficiency and dental anomalies.〔(Steroid dehydrogenase deficiency - dental anomalies Symptoms, Diagnosis, Treatments and Causes - RightDiagnosis.com )〕
== 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".

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
ウィキペディアで「Lyngstadaas syndrome」の詳細全文を読む



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