Cardiocranial syndrome, Pfeiffer type (Q94134): Difference between revisions
From determinar.ia.br - Determine suas informações
Changed label, description and/or aliases in pt-br, en |
Changed an Item |
||
| Property / Canonical URI | |||
| Property / Canonical URI: https://id.who.int/icd/entity/629231429 / rank | |||
Normal rank | |||
Revision as of 09:15, 16 August 2026
Pfeiffer-type cardiocranial syndrome is an extremely rare disorder characterised by a congenital heart defect, sagittal craniosynostosis and severe developmental delay (growth retardation and intellectual deficit). Genital and renal anomalies, and various dysmorphic features (hypertelorism, low set ears, dysplastic ears, micrognathia, mandibular ankylosis, syndactyly) may be present.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_629231429 |
||
| English | Cardiocranial syndrome, Pfeiffer type |
Pfeiffer-type cardiocranial syndrome is an extremely rare disorder characterised by a congenital heart defect, sagittal craniosynostosis and severe developmental delay (growth retardation and intellectual deficit). Genital and renal anomalies, and various dysmorphic features (hypertelorism, low set ears, dysplastic ears, micrognathia, mandibular ankylosis, syndactyly) may be present. |
