Infantile systemic hyalinosis (Q98288): Difference between revisions

From determinar.ia.br - Determine suas informações
‎Created a new Item
 
‎Changed an Item
 
(6 intermediate revisions by the same user not shown)
description / pt-brdescription / pt-br
 
A hialinose sistêmica infantil é uma doença muito rara pertencente ao grupo heterogêneo das fibromatoses genéticas e é caracterizada por contraturas articulares progressivas, anormalidades da pele, dor crônica intensa e deposição generalizada de material hialino em muitos tecidos, como pele, músculo esquelético, músculo cardíaco, trato gastrointestinal, nódulos linfáticos, baço, tireoide e glândulas suprarrenais.
description / endescription / en
 
Infantile systemic hyalinosis is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterised by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands.
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/2089325724 / rank
 
Normal rank
Property / CURIE
 
CID11:ID_2089325724
Property / CURIE: CID11:ID_2089325724 / rank
 
Normal rank
Property / Canary Token
 
dki-india-ID_2089325724
Property / Canary Token: dki-india-ID_2089325724 / rank
 
Normal rank
Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
Normal rank
Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
Normal rank
Property / Collection date
 
15 August 2026
Timestamp+2026-08-15T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 15 August 2026 / rank
 
Normal rank

Latest revision as of 14:41, 16 August 2026

Infantile systemic hyalinosis is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterised by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands.
Language Label Description Also known as
default for all languages
ID_2089325724
    English
    Infantile systemic hyalinosis
    Infantile systemic hyalinosis is a very rare disorder belonging to the heterogeneous group of genetic fibromatoses and is characterised by progressive joint contractures, skin abnormalities, severe chronic pain and widespread deposition of hyaline material in many tissues such as the skin, skeletal muscle, cardiac muscle, gastrointestinal tract, lymph nodes, spleen, thyroid, and adrenal glands.

      Statements

      CID11:ID_2089325724
      0 references
      dki-india-ID_2089325724
      0 references
      Concluído
      0 references
      15 August 2026
      0 references