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Charles I. Jr. Scott
American paediatrician.
Associated eponyms:
Aarskog's syndrome
A familial syndrome combining short stature, abnormal facies, and genital and hand and foot abnormalities.
Hecht-Scott syndrome (Jacqueline T. Hecht)
A syndrome characterised by terminal transverse defects of the limbs associated with congenital heart malformations.
Biography:
Charles I. Scott, Jr. graduated from the University of Arkansas School of Medicine, where he subsequently spent his residency in paediatrics. His certification is from the American Board of Pediatrics; American Board of Medical Genetics.
Scott, Jr. is a fellow of Medical Genetics, Johns Hopkins; and University of Birmingham Children's Hospital, Birmingham, England. He is professor of paediatrics, Jefferson Medical College, and a medical geneticist at the Alfred I. duPont Institute, Wilmington, Delaware.
Bibliography:
- C. I. Scott Jr:
Unusual facies, joint hypermobility, genital anomaly and short stature. A new dysmorphic syndrome.
In: D. Bergsma, V. A. McKusick,, B. W. Konigsmark (eds): The Clinical Delineation of Birth Defects. Vol 10, The Endocrine System, Baltimore 1971, pp 240-246.
Or is it in: Birth Defects Original Article Series, New York, 1971, 7: 260-246.
Aarskog-Scott syndrome.
- W. A. Horton, Judith G. Hall, C. I. Scott, R. E. Pyeritz, and David Lawrence Rimoin:
Growth Curves for Height for Diastrophic Dysplasia. Spondyloepiphyseal Dysplasia Congenita, and Pseudoachondroplasia.
American Journal of Diseases of Children, Chicago, 1982, 138 (April): 316-319.
- W. A. Horton, J. I. Potter, D. L. Rimoin, C. I. Scott, J. G. Hall:
Standard growth curves for achondroplasia.
Journal of Pediatrics, St. Louis, 1978, 93: 435-438.
- M. Deere, S. H. Blanton, C. I. Scott, Leonard O. Langer Jr, R. M. Pauli and J. T. Hecht:
Genetic heterogeneity in multiple epiphyseal dysplasia.
The American Journal of Human Gentics, Chicago, 1995, 56: 698-704.
- Gerald A. Mandell, H. Theodore Harcke, C. I. Scott, Pilar A. Caro, Harry J. Einsig, J. Richard Bowen:
Protrusio Acetabuli in Neurofibromatosis: Nondysplastic and Dysplastic Forms.
Neurosurgery, Baltimore, 1992, 30 (4): 552.
- J. E. Parrish, M. J. Wagner, J. T. Hecht, C. I. Scott and D. E. Wells:
Molecular analysis of overlapping chromosomal deletions in patients with Langer-Giedion Syndrome.
Genomics, Sand Diego, 1991, 11: 54-61.
- L. O. Langer Jr., Rodney Kenneth Beals, C. I. Scott Jr.:
Sponastrime dysplasia: diagnostic criteria based on five new and six previously published cases.
Pediatric Radiology, Berlin, 1997, 27 (5), 409-414. Abstract.
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