A newly recognized syndrome of cutis aplasia, lipomatous footpads, microcephaly, hypotelorism, and, variably, single maxillary central incisor, and holoprosencephaly

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Bibliographic Details
Published in:American journal of medical genetics. Part A 2005-08, Vol.136A (4), p.354-356
Main Authors: Basel, Donald, Sklar, Diane, Viljoen, Denis
Format: Article
Language:English
Subjects:
Abnormalities, Multiple - genetics
Abnormalities, Multiple - pathology
Child, Preschool
Cleft Lip - pathology
Craniofacial Dysostosis - pathology
Ectodermal Dysplasia - pathology
Family Health
Female
Foot Diseases - pathology
Genes, Dominant
Holoprosencephaly - pathology
Humans
Incisor - abnormalities
Lipomatosis - pathology
Male
Maxilla
Pedigree
Syndrome
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ISSN:1552-4825
1552-4833
DOI:10.1002/ajmg.a.30629