Hereditary renal adysplasia. Apropos of 2 families
Palcoux, J.B.; Amram, D.; Vanlieferinghen, P.; Pignodel, C.; Chapuis, H.; Malpuech, G.
Archives Francaises de Pediatrie 42(9): 783-784
1985
ISSN/ISBN: 0003-9764 PMID: 4083980 Document Number: 257611
Two families with hereditary renal adysplasia are reported. Transmission is dominant autosomal. There were no genital abnormalities.
Document emailed within 1 workday
Related Documents
Doray, B.; Gasser, B.; Reinartz, I.; Stoll, C. 1999: Hereditary renal adysplasia in a three generations family Genetic Counseling 10(3): 251-257Vasen, H.F.; Müller, H. 1991: DNA studies in families with hereditary forms of cancer Nederlands Tijdschrift Voor Geneeskunde 135(36): 1620-1623
Jusić, A.; Sostarko, M. 1976: Hereditary persistent distal cramps in 2 additional families Neuropsihijatrija 24(1-4): 75-81
Levin, T.; Reichelt, J.; Heimdal, K.; Møller, P. 2001: Information to families with hereditary breast and ovarian cancer Tidsskrift for den Norske Laegeforening: Tidsskrift for Praktisk Medicin Ny Raekke 121(28): 3292-3294
Gnamey, D.; Walbaum, R.; Saint-Aubert, P.; Fontaine, G. 1971: Type C hereditary brachydactyly. Clinical and genetic study of 3 families Annales de Pediatrie 18(6): 438-449
Hlavatý, T.; Lukác, L.'; Duris, I. 2004: Families at risk of colon cancer II. Hereditary nonpolyposis colorectal carcinoma Vnitrni Lekarstvi 50(8): 606-614
Broekmans, A.W.; Bertina, R.M.; Reinalda-Poot, J.; Engesser, L.; Muller, H.P.; Leeuw, J.A.; Michiels, J.J.; Brommer, E.J.; Briët, E. 1985: Hereditary protein S deficiency and venous thrombo-embolism. a study in three Dutch families Thrombosis and Haemostasis 53(2): 273-277
Pasanen, A.V.; Salmi, M.; Tenhunen, R.; Vuopio, P. 1982: Haema synthesis during pyridoxine therapy in two families with different types of hereditary sideroblastic anaemia Annals of Clinical Research 14(2): 61-65
Meire, G.M.; Cochaux, P.; Candaele, C.; Broux, C. 1994: Clinical and genetical manifestations in 34 families with Leber's hereditary optic neuropathy (LHON) Bulletin de la Societe Belge d'Ophtalmologie 254: 137-146
Kostyk, E.; Wieckiewicz, J.; Sutkowska, A.; Zygulska-Mach, H.; Pietrzyk, J.J. 1994: Molecular analysis of alleles segregation at RFLPs within RB-1 gene in four families with hereditary retinoblastoma Materia Medica Polona. Polish Journal of Medicine and Pharmacy 26(3): 105-108
Tannergård, P.; Lipford, J.R.; Kolodner, R.; Frödin, J.E.; Nordenskjöld, M.; Lindblom, A. 1995: Mutation screening in the hMLH1 gene in Swedish hereditary nonpolyposis colon cancer families Cancer Research 55(24): 6092-6096
Bratt, O.; Abrahamsson, P.A.; Lundgren, R.; Olsson, H.; Kristoffersson, U. 1998: Research progress on hereditary prostatic cancer. Families at risk should be surveyed and screening should be offered Lakartidningen 95(14): 1494-1496
Ben Ahméd, S.; Monastiri, K.; Chouchane, L.; el Ouali, M.; Korbi, S.; Kraiem, C.; Khairi, H.; Bignon, Y.J. 1997: Hereditary predisposition to breast cancer: epidemiologic and clinico-anatomic features in 11 Tunisian families La Tunisie Medicale 75(3): 111-116
Cierniková, S.; Tomka, M.; Kovác, M.; Stevurková, V.; Zajac, V. 2006: Ashkenazi founder BRCA1/BRCA2 mutations in Slovak hereditary breast and/or ovarian cancer families Neoplasma 53(2): 97-102
Von Fellenberg, J.; Paternotte, C.; Prud'homme, J.F.; Weissenbach, J.; Hazan, J.; Burgunder, J.M. 1998: Clinical and molecular genetic analysis of 4 Swiss families with the pure form of hereditary spastic spinal paralysis Schweizerische Medizinische Wochenschrift 128(26): 1043-1050
Schwartz, M.; Nørby, S.; Brandt, N.J. 1985: DNA markers, genetic counseling and prenatal diagnosis of hereditary disease. a study of 3 families with Duchenne's muscular dystrophy Ugeskrift for Laeger 147(26): 2071-2075
Bayoudh, F.; Landthaler, G.; Hue, G.; Hecketsweiler, B.; Mallet, E. 1989: Hereditary hyperoxaluria or oxalosis. Apropos of a case Annales de Pediatrie 36(5): 321-325
Lerman, C.; Narod, S.; Schulman, K.; Hughes, C.; Gomez-Caminero, A.; Bonney, G.; Gold, K.; Trock, B.; Main, D.; Lynch, J.; Fulmore, C.; Snyder, C.; Lemon, S.J.; Conway, T.; Tonin, P.; Lenoir, G.; Lynch, H. 1996: BRCA1 testing in families with hereditary breast-ovarian cancer. A prospective study of patient decision making and outcomes JAMA 275(24): 1885-1892
Meddeb, B.; Hafsia, R.; Ben Abid, H.; Guezail, W.; Hafsia, A.; M'Timet, B.; Boussen, M. 1989: Genetic study of congenital afibrinogenemia: apropos of 7 families La Tunisie Medicale 67(5): 315-319
Robert, J.; Pernod, J.; Bonnet, R. 1974: Familial sacro-coccygeal agenesis. Apropos of 6 cases in 2 families Journal de Genetique Humaine 22(1): 45-60