Heart-hand syndrome type 1 (Q105610): Difference between revisions
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Síndrome coração-mão tipo 1 (síndrome de Holt-Oram) é caracterizada por defeitos cardíacos congênitos leves a graves (comunicação interatrial ostium secundum (CIA), comunicação interventricular (CIV) e ostium primum) e anormalidades esqueléticas de membros superiores (anormalidades do raio radial, rádio anormal ou ausente, elementos transversais do membro superior ausentes e várias anomalias do polegar). | |||
| description / en | description / en | ||
Heart-hand syndrome type 1 (Holt-Oram syndrome) is characterised by mild-to-severe congenital cardiac defects (ostium secundum atrial septal defect (ASD), ventricular septal defect (VSD) and ostium primum ASD) and skeletal abnormalities of the upper limbs (radial ray abnormalities, absent or abnormal radius, upper limb-transverse elements missing and various thumb anomalies). | |||
Revision as of 11:57, 17 August 2026
Heart-hand syndrome type 1 (Holt-Oram syndrome) is characterised by mild-to-severe congenital cardiac defects (ostium secundum atrial septal defect (ASD), ventricular septal defect (VSD) and ostium primum ASD) and skeletal abnormalities of the upper limbs (radial ray abnormalities, absent or abnormal radius, upper limb-transverse elements missing and various thumb anomalies).
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1169240278 |
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| English | Heart-hand syndrome type 1 |
Heart-hand syndrome type 1 (Holt-Oram syndrome) is characterised by mild-to-severe congenital cardiac defects (ostium secundum atrial septal defect (ASD), ventricular septal defect (VSD) and ostium primum ASD) and skeletal abnormalities of the upper limbs (radial ray abnormalities, absent or abnormal radius, upper limb-transverse elements missing and various thumb anomalies). |
