Heart-hand syndrome type 2 (Q105608): Difference between revisions
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Síndrome coração-mão tipo 2 é uma síndrome coração-mão extremamente rara descrita em duas famílias até o momento, que é caracterizada por malformações dos membros superiores (braquitelefalangia tipo D, deltóides hipoplásicos, leve encurtamento do quarto e quinto metacarpos em alguns indivíduos, anomalias esqueléticas em úmero, rádio, ulna e ossos tenares) e arritmias cardíacas (ritmos juncionais e fibrilação atrial). | |||
| description / en | description / en | ||
Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterised by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation). | |||
Revision as of 11:56, 17 August 2026
Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterised by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2111612055 |
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| English | Heart-hand syndrome type 2 |
Heart-hand syndrome type 2 is an extremely rare heart-hand syndrome described in two families to date, that is characterised by upper limb malformations (brachytelephalangy type D, hypoplastic deltoids, mild shortening of the fourth and fifth metacarpals in some individuals, skeletal anomalies in the humerus, radius, ulnae, and thenar bones) and cardiac arrhythmias (junctional rhythms and atrial fibrillation). |
