A newly recognized syndrome of cutis aplasia, lipomatous footpads, microcephaly, hypotelorism, and, variably, single maxillary central incisor, and holoprosencephaly. Am J Med Genet A 2005 Aug 01;136A(4):354-6
Date
06/23/2005Pubmed ID
15971262DOI
10.1002/ajmg.a.30629Scopus ID
2-s2.0-23044507713 (requires institutional sign-in at Scopus site) 1 CitationAuthor List
Basel D, Sklar D, Viljoen DAuthor
Donald Basel MD Chief, Professor in the Pediatrics department at Medical College of WisconsinMESH terms used to index this publication - Major topics in bold
Abnormalities, MultipleChild, Preschool
Cleft Lip
Craniofacial Dysostosis
Ectodermal Dysplasia
Family Health
Female
Foot Diseases
Genes, Dominant
Holoprosencephaly
Humans
Incisor
Lipomatosis
Male
Maxilla
Pedigree
Syndrome