Encephalocraniocutaneous lipomatosis (Q90781): Difference between revisions

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Lipomatose encefalocraniocutânea é uma síndrome neurocutânea esporádica rara envolvendo tecidos de origem ectodérmica e mesodérmica e caracterizada por déficit intelectual profundo, início precoce de convulsões, lipomatose temporofrontal unilateral, lipomatose cerebral e leptomeningeal ipsilateral, malformação e calcificação cerebrais, e lipomas do crânio, do olho e do coração.
description / endescription / en
 
Encephalocraniocutaneous lipomatosis is a rare sporadic neurocutaneous syndrome involving tissues of ectodermal and mesodermal origin and characterised by profound mental retardation, early onset of seizures, unilateral temporofrontal lipomatosis, ipsilateral cerebral and leptomeningeal lipomatosis, cerebral malformation and calcification, and lipomas of the skull, eye, and heart.
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Property / Canonical URI: https://id.who.int/icd/entity/1084215843 / rank
 
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Property / CURIE
 
CID11:ID_1084215843
Property / CURIE: CID11:ID_1084215843 / rank
 
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Property / Canary Token
 
dki-india-ID_1084215843
Property / Canary Token: dki-india-ID_1084215843 / rank
 
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Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Latest revision as of 17:46, 15 August 2026

Encephalocraniocutaneous lipomatosis is a rare sporadic neurocutaneous syndrome involving tissues of ectodermal and mesodermal origin and characterised by profound mental retardation, early onset of seizures, unilateral temporofrontal lipomatosis, ipsilateral cerebral and leptomeningeal lipomatosis, cerebral malformation and calcification, and lipomas of the skull, eye, and heart.
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ID_1084215843
    English
    Encephalocraniocutaneous lipomatosis
    Encephalocraniocutaneous lipomatosis is a rare sporadic neurocutaneous syndrome involving tissues of ectodermal and mesodermal origin and characterised by profound mental retardation, early onset of seizures, unilateral temporofrontal lipomatosis, ipsilateral cerebral and leptomeningeal lipomatosis, cerebral malformation and calcification, and lipomas of the skull, eye, and heart.

      Statements

      CID11:ID_1084215843
      0 references
      dki-india-ID_1084215843
      0 references
      Concluído
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      13 August 2026
      0 references