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Roberta A. Pagon
US paediatrician and geneticist.
Associated eponyms:
Pagon's syndrome
Congenital anaemia with ataxia, clonus, and positive Babinski sign.
Walker-Warburg syndrome
A lethal disorder of the brain marked by hydrocephalus, cerebral agyria, retinal dysplasia and other eye abnormalities, and occasional occipital encephalocele.
Biography:
We thank Andre Trombeta for information submitted.
Bibliography:
- R. A. Pagon, D. W. Smith, Th. H. Shephard:
Urethral obstruction malformation complex: a cause of abdominal muscle deficiency and the "prune belly".
Journal of Pediatrics, St. Louis, 1979, 94: 900. 1979;
IBID: 1979, 96: 776-777 (Letters to the editor).
- A. H. Bunt-Milam, R.E. Kalina, and R.A. Pagon:
Clinical-ultrastructural study of a retinal dystrophy.
Investigative Ophthalmology and Visual Science, 1983, 24:458-469.
- R. A. Pagon:
Teschler-Nicola/Killian syndrome.
Journal of Clinical Dysmorphology, London, 1983, 1(3):18-9.
- R.A. Pagon, J. Allanson, S. Shulman, M. Barr, V. McGravey, C. Dabiri, N. Schimke, E. Ives and B.D. Hall:
Smith-Lemli-Opitz syndrome-type II: multiple congenital anomalies with male pseudohermaphroditism and frequent early lethality.
American Journal of Medical Genetics, 1987, 26: 45-57.
- T. D. Wardinsky, E. Weinberger, R. A. Pagon, S. K. Clarren and H. C. Thuline:
Partial deletion of the long arm of chromosome 11 [del(11)(q23.3-qter)] with abnormal white matter.
American Journal of Medical Genetics, New York, 1990, 35:60-63.
- W.B. Dobyns, E.R. Elias, A.C. Newlin, R.A. Pagon, D.H. Ledbetter:
Causal Heterogeneity in Isolated Lissencephaly.
Neurology, 1992, 42 (July 7): 1375
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