Landau–Kleffner syndrome
a rare childhood neurological syndrome characterized by seizures and progressive loss of speech typically in a child with previous age-appropriate development
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Landau–Kleffner syndrome
Summary
Landau–Kleffner syndrome is a designated intractable/rare disease[1]. It has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Landau–Kleffner syndrome's instance of is recorded as designated intractable/rare disease[3].
- Landau–Kleffner syndrome's instance of is recorded as rare disease[4].
- Landau–Kleffner syndrome's instance of is recorded as class of disease[5].
- William Landau is named after Landau–Kleffner syndrome[6].
- Frank Kleffner is named after Landau–Kleffner syndrome[7].
- Landau–Kleffner syndrome is a type of childhood electroclinical syndrome[8].
- Landau–Kleffner syndrome is a type of disease[9].
- Landau–Kleffner syndrome's external data available at URL is recorded as http://www.nanbyou.or.jp/entry/4411[10].
- Landau–Kleffner syndrome's NCI Thesaurus ID is recorded as C84806[11].
- Landau–Kleffner syndrome's health specialty is recorded as neurology[12].
- Landau–Kleffner syndrome's health specialty is recorded as psychiatry[13].
- Landau–Kleffner syndrome's genetic association is recorded as GRIN2A[14].
- Landau–Kleffner syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_2538[15].
- Landau–Kleffner syndrome's exact match is recorded as http://identifiers.org/doid/DOID:2538[16].
- Landau–Kleffner syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Landau–Kleffner syndrome has Wikipedia articles in 15 language editions, a strong signal of global cultural recognition.[2] It is known by 15 alternative names across languages and contexts.[18]