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Skeletal and cardiac malformations with thrombocytopenia: a new syndrome?
R Rupps1, A M Elliott, E M Azouz
1F. Clarke Fraser Clinical Genetics Unit, Montreal Children's Hospital, Quebec, Canada.
American Journal of Medical Genetics
|August 23, 1996
Abstract:
We describe a female patient with multiple anomalies suggestive of a new syndrome. Manifestations include: VSD and ASD, mild developmental delay, conductive hearing loss, minor facial anomalies, thrombocytopenia, and radiological findings (including carpal fusion). Some of these manifestations may be present in the Keutel syndrome, IVIC syndrome, and the 10qter deletion syndrome. However, none of these syndromes can explain the spectrum of anomalies seen in our patient.