Thanatophoric dysplasia (Q46595): Difference between revisions

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A displasia tanatofórica é um distúrbio esquelético grave que é letal no período neonatal. Dois subtipos clinicamente definidos de TD foram classificados: tipo I (TDI), caracterizado por micromelia com fêmures arqueados e, ocasionalmente, pela presença de deformidade craniana em folha de trevo de gravidade variável e tipo II (TDII), caracterizada por micromelia com fêmures retos e um deformidade craniana em "folha de trevo" moderada a grave.
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Thanatophoric Dysplasia is a severe skeletal disorder that is lethal in the neonatal period. Two clinically defined TD subtypes have been classified: type I (TDI), characterised by micromelia with bowed femurs and, occasionally, by the presence of cloverleaf skull deformity of varying severity and type II (TDII), characterised by micromelia with straight femurs and a moderate to severe cloverleaf skull deformity.

Revision as of 15:16, 13 August 2026

Thanatophoric Dysplasia is a severe skeletal disorder that is lethal in the neonatal period. Two clinically defined TD subtypes have been classified: type I (TDI), characterised by micromelia with bowed femurs and, occasionally, by the presence of cloverleaf skull deformity of varying severity and type II (TDII), characterised by micromelia with straight femurs and a moderate to severe cloverleaf skull deformity.
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    English
    Thanatophoric dysplasia
    Thanatophoric Dysplasia is a severe skeletal disorder that is lethal in the neonatal period. Two clinically defined TD subtypes have been classified: type I (TDI), characterised by micromelia with bowed femurs and, occasionally, by the presence of cloverleaf skull deformity of varying severity and type II (TDII), characterised by micromelia with straight femurs and a moderate to severe cloverleaf skull deformity.

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