Cardioskeletal syndromes (Q94121): Difference between revisions
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Síndromes cardioesqueléticas (síndrome coração-mão) refere-se a um grupo de transtornos congênitos caracterizados por malformações dos membros superiores e do coração. Até o momento, a síndrome coração-mão compreende as seguintes síndromes raras; Síndrome de Holt-Oram; síndrome coração-mão tipo 2; síndrome coração-mão tipo 3; síndrome coração-mão, tipo esloveno, braquidactilia-polegar longo; e persistência do canal arterial-valva aórtica bicúspide - anomalias nas mãos. | |||
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Cardioskeletal syndromes (Heart-hand syndrome) refers to a group of congenital disorders characterised by malformations of the upper limbs and heart. To date, heart-hand syndrome comprises the following rare syndromes; Holt-Oram syndrome; heart-hand syndrome type 2; heart-hand syndrome type 3; heart hand syndrome, Slovenian type, brachydactyly-long thumb; and patent ductus arteriosus-bicuspid aortic valve - hand anomalies. | |||
Revision as of 09:14, 16 August 2026
Cardioskeletal syndromes (Heart-hand syndrome) refers to a group of congenital disorders characterised by malformations of the upper limbs and heart. To date, heart-hand syndrome comprises the following rare syndromes; Holt-Oram syndrome; heart-hand syndrome type 2; heart-hand syndrome type 3; heart hand syndrome, Slovenian type, brachydactyly-long thumb; and patent ductus arteriosus-bicuspid aortic valve - hand anomalies.
| Language | Label | Description | Also known as |
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| default for all languages | ID_1364474053 |
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| English | Cardioskeletal syndromes |
Cardioskeletal syndromes (Heart-hand syndrome) refers to a group of congenital disorders characterised by malformations of the upper limbs and heart. To date, heart-hand syndrome comprises the following rare syndromes; Holt-Oram syndrome; heart-hand syndrome type 2; heart-hand syndrome type 3; heart hand syndrome, Slovenian type, brachydactyly-long thumb; and patent ductus arteriosus-bicuspid aortic valve - hand anomalies. |
