Heart-hand syndrome type 1 (Q105610): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed an Item |
Changed an Item |
||
| Property / Knowledge Architect | |||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||
Normal rank | |||
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 |
||
| 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). |
Statements
CID11:ID_1169240278
0 references
dki-india-ID_1169240278
0 references
Concluído
0 references
