Opitz trigonocephaly syndrome: Report of two cases View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

1984-01

AUTHORS

S. D. Flatz, A. Schinzel, E. Doehring, D. Kamran, E. Eilers

ABSTRACT

We report two patients with Opitz trigonocephaly syndrome. Both children showed the pattern of abnormal findings characteristic of this syndrome, including trigonocephaly, upslanted palpebral fissures, inner epicanthic folds, broad alveolar ridges, small chin, short neck with loose skin, muscular hypotonia and cardiac defect. An 8-week-old girl had multiple gingival frenula, brachydactyly, syndactyly of toes and anal stenosis in addition, while a boy who died at 28 h from cardiac failure showed multiple joint contractures, cryptorchidism and renal cortical cysts. More... »

PAGES

183-185

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/bf00443223

DOI

http://dx.doi.org/10.1007/bf00443223

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1019345171

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/6698065


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