Cardiocranial syndrome, Pfeiffer type
Synonyms: Craniosynostosis-congenital heart disease-intellectual disability syndrome | Pfeiffer-Singer-Zschiesche syndrome
A rare multiple congenital anomalies syndrome with intellectual disability commonly characterized by facial dysmorphism (e.g. sagittal craniosynostosis hypertelorism strabismus low-set dysplastic ears retrognathia or micrognathia mandibular ankyloses cleft palate aplasia uvulae) congenital heart defects (e.g. atrioventricular septal defect anomalous venous return) genital anomalies (e.g. cryptorchidism microphallus) as well as growth delay and intellectual disability. In some cases tracheobronchial anomalies large joint contractures syndactyly rib anomalies and hypoplastic kidneys are reported. Rarely no cardiac anomaly may be reported.
Data from Orphanet are used to provide information on a disease's name, synonym(s), and overview.
Reference: Access aggregated data from Orphanet at Orphadata.
Orphadata: Free access data from Orphanet. © INSERM 1999. Available on http://www.orphadata.org. Data version April 2024
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Cardiocranial syndrome, Pfeiffer type?
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Advocacy Organizations
COMBINEDBrain Inc
COMBINEDBrain is a consortium for outcome measures and biomarkers for neurodevelopmental disorders. We are collaborating to cure rare, non-verbal brain disorders.
DDX3X Foundation
Our mission is to connect families, resources, and the medical community to advance research for a treatment or cure to DDX3X Syndrome. Our ultimate goal is to accelerate brain function in individuals affected by DDX3X Syndrome through advances in cell and gene therapy and pharmaceuticals.
Moonshots for Unicorns
Curing single-gene disorders
Project CASK
To fund research for treatment and/or a cure for CASK Gene Disorder
Syndromes Without A Name (SWAN) Australia
Provide information, support and advocacy to families caring for a child with an undiagnosed or rare genetic condition.
Clinical Trials
For a list of clinical trials in this disease area, please click here.