PubMed · 5259541
The source did not provide an abstract. Follow the original record for more information.
Explore connections, maps & timelines
R Vossmerbäumer. 1969-10-25. [Case report on missing permanent lower cuspids].. https://pubmed.ncbi.nlm.nih.gov/5259541/
Cite the original work for its findings. Save a collection to share your selection of sources.
KEEP EXPLORING
Schöpf-Schulz-Passarge syndrome is a rare form of ectodermal dysplasia comprising hypotrichosis, hypodontia, unusual eyelid cysts, palmar-plantar keratosis, and nail dystrophy. To date, ten cases have been reported; all except one are compatible with autosomal recessive inheritance. We report on a family in which three full sibs and one half-sib have Schopf-Schulz-Passarge syndrome, yet there is no other evidence of dominant transmission in prior or subsequent generations. Possible explanations are discussed.
Explore the source record for details and available documents.