Infantile systemic hyalinosis (Q98288): Difference between revisions
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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 / en | description / 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. | |||
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 |
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| 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. |
