Related Experiment Videos
Scalp defects, polythelia, microcephaly, and developmental delay: a new syndrome with apparent autosomal dominant
Michael Marble1, Gabriella Pridjian
1Human Genetics Program, Hayward Genetics Center and Department of Pediatrics, Tulane University School of Medicine, New Orleans, Louisiana, USA. mmarble@bellsouth.net
American Journal of Medical Genetics
|March 29, 2002
Abstract:
We report a family with apparent autosomal dominant inheritance of scalp defects, polythelia, microcephaly, and developmental delay. A review of the literature revealed no previous report of this combination of anomalies. We conclude that these patients have a new autosomal dominant syndrome.