Noonan syndrome

Journal of Medical Genetics

Volumn 24, Issue 1, 1987, Pages 9-13

  Allanson, J E ^a  

^a Southwest Biomedical Research Institute   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

CARDIOVASCULAR SYSTEM; CENTRAL NERVOUS SYSTEM; CLINICAL FEATURE; CONGENITAL DISORDER; CONGENITAL HEART MALFORMATION; DIAGNOSIS; ETIOLOGY; FACE DYSMORPHIA; GROWTH RETARDATION; HEART; HEREDITY; HUMAN; NOONAN SYNDROME; PRIORITY JOURNAL; SHORT SURVEY;

EID: 0023133725     PISSN: 00222593     EISSN: None     Source Type: Journal    
DOI: 10.1136/jmg.24.1.9     Document Type: Review

References (39)

1. Noonan, J.A.; Ehmke, D.A. Associated noncardiac malformations in children with congenital heart disease J Pediatr 1963 63 46870
2. 0, Kobylinski Ueber eine flughautahnliche Ausbreitung am Haise Arch Anthropol 1883 342 14
3. Nora, J.J.; Fraser, F.C. Medical genetics: principles and practice 2nd ed 1981
4. Mendez, H.M.M.; Opitz, J.M. Noonan syndrome: a review Am J Med Genet 1985 10.1002/ajmg.1320210312 21 493
5. Nora, J.J.; Nora, A.H.; Sinha, A.K.; Spangler, R.D.; Lubs, H.A. The Ullrich-Noonan syndrome (Turner phenotype) Am J Dis Child 1974 127 48
6. Char, F.C.; Rodriguez-Fernandez, H.L.; Scott, C.I.; Borgaonkar, D.S.; Bell, B.B.; Rowe, R.D. The Noonan syndrome-a clinical study of forty-five cases Birth Defects 1972 5 110
7. Pearl, W. Cardiovascular anomalies in Noonan's syndrome Chest 1977 10.1378/chest.71.5.677 71 677
8. Elders, M.J.; Char, F. Possible etiologic mechanisms of the short stature in Noonan syndrome Birth Defects 1976 6 127
9. Witt, D.R.; Keena, B.A.; Hall, J.G.; Allanson, J.E. Growth curves for height in Noonan syndrome
10. Allanson, J.E.; Hall, J.G.; Hughes, H.E.; Preus, M.; Witt, R.D. Noonan syndrome: the changing phenotype Am J Med Genet 1985 10.1002/ajmg.1320210313 21 507
11. Sanchez-Cascos, A. The Noonan syndrome Eur Heart J 1983 10.1093/oxfordjournals.eurheartj.a061452 4 223
12. Pierini, D.O.; Pierini, A.M. Keratosis pilaris atrophicans faciei (Ulerythema ophryogenes): a cutaneous marker in the Noonan's syndrome Br J Dermatol 1979 10.1111/j.1365-2133.1979.tb01641.x 100 409
13. Allanson, J.E.; Hall, J.G.; Van Allen, M.I. Noonan phenotype associated with neurofibromatosis Am J Med Genet 1985 10.1002/ajmg.1320210307 21 457
14. Kaplan, P.; Rosenblatt, B. A distinctive facial appearance in neurofibromatosis von Recklinghausen Am J Med Genet 1985 10.1002/ajmg.1320210308 21 463
15. Mendez, H.M.M. The neurofibromatosis-Noonan syndrome Am J Med Genet 1985 10.1002/ajmg.1320210309 21 471
16. Kitchens, C.S.; Alexander, J.A. Partial deficiency of coagulation factor XI as a newly recognised feature of Noonan syndrome J Pediatr 1983 10.1016/S0022-3476(83)80525-3 102 224
17. Witt, D.; Allanson, J.; Wadsworth, L.; Hall, J.G. Bleeding disorders in 7 cases of Noonan syndrome: further evidence of heterogeneity Am J Hum Genet 1985 37 83
18. Humbert, JR, Hammond; KB, Hathaway; WE, Marcoux; JG, O.'Brien; D. Trimethylaminuria: the fish-odour syndrome Lancet 1970 ii: 770
19. Witt, D.R.; Hoyme, H.E.; Zonana, J.; Manchester, D.K.; Fryns, J.P.; Hall, J.G. Lymphedema in Noonan syndrome
20. Vesterhus, P.; Aarskog, D. Noonan's syndrome and autoimmune thyroiditis J Pediatr 1973 10.1016/S0022-3476(73)80482-2 83 237
21. Chaves-Carballo, E.; Hayles, A.B. Ullrich-Turner syndrome in the male: review of the literature and report of a case with lymphocytic (Hashimoto's) thyroiditis Mayo Clin Proc 1966 41 843
22. Becker, C.E.; Rosen, S.W.; Engelman, K. Pheochromocytoma and hyporesponsiveness to thyrotropin in a 46, XY male with features of Turner phenotype Ann Intern Med 1969 325 70
23. D, Khodadoust A.Paton Turner's syndrome in a male. Report of a case with myopia, retinal detachment, cataract and glaucoma Arch Ophthalmol 1967 10.1001/archopht.1967.00980020632011 77 630
24. Krieger, I.; Espiritu, C.E. Arthrogryposis multiplex congenita and the Turner phenotype Am J Dis Child 1972 123 141
25. Ball, M.J.; Peiris, A. Chiari (type 1) malformation and syringomyelia in a patient with Noonan's syndrome J Neurol Neurosurg Psychiatry 1982 753 45
26. Nelson, J.F.; Konzelman, Tsaknis P.J.; J.L. Noonan's syndrome: report of a case with oral findings J Oral Med 1978 33 94
27. Kaplan, A.M.; Bergeson, P.S.; Gregg, S.A.; Curless, R.G. Malignant hyperthermia associated with myopathy and normal muscle enzymes J Pediatr 1977 10.1016/S0022-3476(77)81314-0 91 431
28. King, J.O.; Denborough, M.A. Anesthetic-induced malignant hyperpyrexia in children J Pediatr 1973 10.1016/S0022-3476(73)80309-9 83 37
29. Hunter, A.; Pinsky, L. An evaluation of the possible association of malignant hyperpyrexia with Noonan syndrome using serum creatine phosphokinase levels J Pediatr 1975 10.1016/S0022-3476(75)80974-7 96 412
30. Grix, A.; Hall, B.D. Noonan phenotype with polydactyly Birth Defects 1979 5 313
31. Feldman, K.W.; Ochs, H.D.; Price, T.H.; Wedgwood, R.J. Congenital stem cell dysfunction associated with Turner-like phenotype J Pediatr 1976 10.1016/S0022-3476(76)81055-4 88 979
32. Krishan, E.U.; Wegner, K.; Garg, S.K. Congenital hypoplastic anemia terminating in acute promyelocytic leukemia Pediatrics 1978 61 898
33. Familial Williams syndrome
34. R, Myhre S.A.Williams Teratogenic effects associated with maternal primidone therapy J Pediatr 1981 10.1016/S0022-3476(81)80986-9 99 160
35. Clericuzio, C. Fetal primidone effects. Proc Greenwood Gen Cen 1985; 4 93
36. Spiegel, P.G.; Pekman, W.M.; Rich, B.H.; Versteeg, C.N.; Nelson, V.; Dudnikov, M. The orthopedic aspects of the fetal alcohol syndrome Clin Orthop 1979 139 58
37. Escobar, V.; Weaver, D.D. Aarskog syndrome. New findings and genetic analysis JAMA 1978 10.1001/jama.1978.03290240038020 240 2638
38. Clark, E.B. Mechanisms in the pathogenesis of congenital heart defects. Proc Greenwood Gen Cen 1985,4 80
39. Clark, E.B. Neck web and congenital heart defects: a pathogenic association in 45XO Turner syndrome? Teratology 1984 10.1002/tera.1420290305 29 35561