Marden-Walker syndrome (Q85066): Difference between revisions

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A síndrome de Marden-Walker é uma síndrome de anomalias do desenvolvimento caracterizada por múltiplas contraturas articulares congênitas, características dismórficas com uma fase semelhante a máscara, blefarofimose, ptose, micrognatia, fenda ou palato arqueado alto, orelhas de implantação baixa, aracnodactilia, massa muscular diminuída, falha no crescimento e atraso psicomotor.
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Marden-Walker syndrome is a developmental anomalies syndrome characterised by multiple congenital joint contractures, dysmorphic features with a mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high-arched palate, low-set ears, arachnodactyly, decreased muscular mass, failure to thrive and psychomotor retardation.

Revision as of 10:25, 15 August 2026

Marden-Walker syndrome is a developmental anomalies syndrome characterised by multiple congenital joint contractures, dysmorphic features with a mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high-arched palate, low-set ears, arachnodactyly, decreased muscular mass, failure to thrive and psychomotor retardation.
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ID_1983460876
    English
    Marden-Walker syndrome
    Marden-Walker syndrome is a developmental anomalies syndrome characterised by multiple congenital joint contractures, dysmorphic features with a mask-like face, blepharophimosis, ptosis, micrognathia, cleft or high-arched palate, low-set ears, arachnodactyly, decreased muscular mass, failure to thrive and psychomotor retardation.

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