Premium
COLOBOMATA OF THE IRIS, CILIARY BODY AND CHOROID IN AN INFANT WITH OESOPHAGO‐TRACHEAL FISTULA AND CONGENITAL HEART DEFECTS. AN UNKNOWN MALFORMATION COMPLEX
Author(s) -
LILLQUIST K.,
WARBURG M.,
ANDERSEN S. RY,
HÄGERSTRAND I.
Publication year - 1980
Publication title -
acta pædiatrica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.772
H-Index - 115
eISSN - 1651-2227
pISSN - 0803-5253
DOI - 10.1111/j.1651-2227.1980.tb07106.x
Subject(s) - medicine , iris (biosensor) , fistula , ciliary body , choroid , anatomy , ophthalmology , surgery , retina , physics , computer security , computer science , biometrics , optics
. Lillquist, K., Warburg, M., Ry Andersen, S. and Hägerstrand, I. (Paediatric Department, Odense University Hospital, The Copenhagen Eye Clinic for the Mentally Retarded, The Institute of Eye Pathology in Copenhagen and Pathological Institute, Odense University Hospital, Denmark). Colobomata of the iris, ciliary body and choroid in an infant with oesophago‐tracheal fistula and congenital heart defects. An unknown malformation complex. Acta Paediatr Scand, 69:417, 1980.—A malformation pattern, not previously reported consisting of microphthalmia, uveal coloboma, oesophago‐tracheal fistula and congenital heart defects is presented. The phaenotypical similarity and difference from previously reported cases are discussed.