Rapp-Hodgkin ectodermal dysplasia syndrome
- 1 October 1981
- journal article
- research article
- Published by BMJ in Archives of Disease in Childhood
- Vol. 56 (10) , 793-795
- https://doi.org/10.1136/adc.56.10.793
Abstract
A mother and daughter with Rapp-Hodgkin ectodermal dysplasia syndrome are reported. Features of the previously described cases were confirmed, although no growth deficiencies were observed. Autosomal dominant inheritance was probable although X-linked transmission could not be excluded.This publication has 4 references indexed in Scilit:
- Ectodermal dysplasia and multiple defects (Rapp-Hodgkins type)The Journal of Pediatrics, 1972
- Hypohidrotic ectodermal dysplasia with multiple associated anomalies.1971
- Anhidrotic ectodermal dysplasia: autosomal dominant inheritance with palate and lip anomalies.Journal of Medical Genetics, 1968
- Diminished sweat pores in hypohidrotic ectodermal dysplasia: A new method for assessmentThe Journal of Pediatrics, 1968