Adams-Oliver syndrome (Q94109): Difference between revisions

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A síndrome de Adams-Oliver é um transtorno raro caracterizado pela combinação de anormalidades congênitas de membros e defeitos no couro cabeludo, frequentemente acompanhados por defeitos de ossificação do crânio. Aplasia cutis congênita, defeitos transversos de membros e cútis marmorata telangiectásica são características dessa condição.
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Adams-Oliver Syndrome is a rare disorder characterised by the combination of congenital limb abnormalities and scalp defects, often accompanied by skull ossification defects. Aplasia cutis congenita, transverse limb defects and cutis marmorata telangiectica are characteristic of this condition.

Revision as of 09:13, 16 August 2026

Adams-Oliver Syndrome is a rare disorder characterised by the combination of congenital limb abnormalities and scalp defects, often accompanied by skull ossification defects. Aplasia cutis congenita, transverse limb defects and cutis marmorata telangiectica are characteristic of this condition.
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    Adams-Oliver syndrome
    Adams-Oliver Syndrome is a rare disorder characterised by the combination of congenital limb abnormalities and scalp defects, often accompanied by skull ossification defects. Aplasia cutis congenita, transverse limb defects and cutis marmorata telangiectica are characteristic of this condition.

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