Multiple pterygium syndrome, lethal forms (Q93726): Difference between revisions
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Síndrome de pterígio múltiplo letal (LMPS) é uma associação rara de anomalias de pele, músculos e esqueleto. LMPS é caracterizada por deficiência de crescimento do início pré-natal, pterígio presente em várias áreas (do queixo ao esterno, cervical, axilar, úmero-ulnar, crural, poplítea e dos tornozelos) e contraturas em flexão que dão origem a artrogripose grave. | |||
| description / en | description / en | ||
Lethal multiple pterygium syndrome (LMPS) is a rare association of anomalies of the skin, muscles and skeleton. LMPS is characterised by growth deficiency of prenatal onset, pterygia present in multiple areas (chin to sternum, cervical, axillary, humero-ulnar, crural, popliteal, and the ankles) and flexion contractures giving rise to severe arthrogryposis. | |||
Revision as of 08:49, 16 August 2026
Lethal multiple pterygium syndrome (LMPS) is a rare association of anomalies of the skin, muscles and skeleton. LMPS is characterised by growth deficiency of prenatal onset, pterygia present in multiple areas (chin to sternum, cervical, axillary, humero-ulnar, crural, popliteal, and the ankles) and flexion contractures giving rise to severe arthrogryposis.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1611756128 |
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| English | Multiple pterygium syndrome, lethal forms |
Lethal multiple pterygium syndrome (LMPS) is a rare association of anomalies of the skin, muscles and skeleton. LMPS is characterised by growth deficiency of prenatal onset, pterygia present in multiple areas (chin to sternum, cervical, axillary, humero-ulnar, crural, popliteal, and the ankles) and flexion contractures giving rise to severe arthrogryposis. |
