Hostname: page-component-586b7cd67f-t7fkt Total loading time: 0 Render date: 2024-11-23T02:14:02.596Z Has data issue: false hasContentIssue false

High Rate of Twins among Offspring of Mothers with the Järvi-Hakola-Nasu Disease and with Comments on Disorders Associated with Twinning

Published online by Cambridge University Press:  01 August 2014

H. P. A. Hakola*
Affiliation:
The Department of Forensic Psychiatry, University of Kuopio, Finland
A. W. Eriksson
Affiliation:
Folkhälsan Institute of Genetics, Population Genetics Unit, Helsinki, Finland
*
Niuvanniemi Hospital, University of Kuopio, Department of Forensic Psychiatry, FIN-70240 Kuopio, Finland

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Finnish mothers with Järvi-Hakola-Nasu disease, progressive dementia with lipomembranous polycystic osteodysplasia (McKusick 221770) have a high rate of twin maternities, 128.2/1000. The exact 99% confidence intervals are 28.7 – 322.2/1000, thus above the average twinning rate in Finland, i.e. 15/1000. This eightfold increase in twinning may be an indication of a disturbed cortico-hypothalmic-hypophyseal axis or an other premorbid hormonal imbalance. It is concluded that even if dizygotic twinning is as a rule an event in itself, not only iatrogenic factors, as ovulation inducers, etc., but also some genetic disorders may be associated with twinning. More studies are needed to elucidate the incidence of twinning in families with these disorders.

Type
Research Article
Copyright
Copyright © The International Society for Twin Studies 1997

References

REFERENCES

1.Adolfsson, R, Forsell, A, Johansson, G (1978): Hereditary polycystic osteodysplasia with progressive dementia in Sweden. Lancet ii: 12091210.Google Scholar
2.Ammann, F, Klein, D, Franceschetti, A (1965): Genetic and epidemiological investigations of pigmentary degeneration of the retina and allied disorders in Switzerland. J Neurol Sci 2: 183196.CrossRefGoogle ScholarPubMed
3.Benirschke, K, Kim, CK (1973): Multiple pregnancy. New Engl J Med 288: 1276–1284, 13291336.CrossRefGoogle ScholarPubMed
4.Bird, TD, Koerker, RM, Leaird, BJ, Vlcek, BW, Thorning, DR (1983): Lipomembranous polycystic osteodysplasia (brain, bone, and fat disease): A genetic cause of presenile dementia. Neurology (NY) 33: 8186.Google Scholar
5.Bulmer, MG (1970): The Biology of Twinning in Man. Oxford Univ Press, Oxford & London.Google Scholar
6.Clark, P, Martin, NG (1928): An excess of the Pi allele in dizygotic twins and their mothers. Hum Genet 61: 171174.Google Scholar
7.Côté, GB, Gyftodimou, J (1991): Twinning and mitotic crossing-over: Some possibilities and their implications. Am J Hum Genet 49:120130.Google ScholarPubMed
8.David, TJ, O'Callaghan, SE (1974): Twinning and oesophageal atresia. Arch Dis Child 49:660662.Google Scholar
9.Dolk, H (1991): Methylene blue and atresia or stenosis of ileum and jejunum. Lancet 338:10211022.CrossRefGoogle ScholarPubMed
10.Eriksson, AW (1973): Human twinning in and around the Åland Islands. Commentationes Biologicae 64: 1159.Google Scholar
11.Eriksson, AW (1990): Twinning in families of triplets. Acta Genet Med Gemellol 39:279293.Google ScholarPubMed
12.Eriksson, AW, Fellman, J (1973): Differences in the twinning trends between Finns and Swedes. Amer J Hum Genet 25: 141151.Google ScholarPubMed
13.Eriksson, AW, Fellman, JO (1976): Retrospective studies on the twinning rate in Scandinavia. Acta Genet Med Gemellol 25: 2935.CrossRefGoogle ScholarPubMed
14.Forsius, H, Eriksson, AW (1970): Tapeto-retinal degenerations with varying clinical features in Åland Islanders. J Med Genet 7(3): 200212.Google Scholar
15.Frants, RR (1980): A contribution to the genetics of alpha-1 antitrypsin. Thesis Vrije Universiteit, Amsterdam: 1146.Google Scholar
16.Fryns, JP (1986): The female and the fragile X. A study of 144 obligate female carriers. Am J Med Genet 23: 157169.CrossRefGoogle Scholar
17.Gemzell, CA (1962): Induction of ovulation with human pituitary gonadotrophins. Fertil Steril 13: 153168.CrossRefGoogle ScholarPubMed
18.Hakola, HPA (1972): Neuropsychiatric and genetic aspects of a new hereditary disease characterized by progressive dementia and lipomembranous polycystic osteodysplasia. Acta Psychiatr Scand Suppl. 232: 1173.Google Scholar
19.Hakola, HPA (1990): Polycystic lipomembranous ostedysplasia with sclerosing leukoencecephalopathy (membranous lipodystrophy). Monographs of Psychiatria Fennica 17: 1114.Google Scholar
20.Hakola, HPA (1990): Psychosocial reactions in the spouses of patients suffering polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy. J Clin Psychiatry 51 (1): 2124.Google ScholarPubMed
21.Järvi, OH, Lauttamus, LL, Solonen, KA (1964): Membranous reticulin dysplasia of bones. Probably a new disease entity. Proc of the 14th Scandinav Congr of Pathol and Microbiol, p 51. Universitets förlaget, Oslo.Google Scholar
22.Järvi, O, Hakola, P, Sourander, P, Kormano, M, Nevalainen, T, Kalimo, H (1980): Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (PLO-SL). In Eriksson, AW, Forsius, HR, Nevanlinna, HR, Workman, PL, Norio, RK (eds): Rare diseases and markers in Finland, p 656664. Academic Press, London-New York-Toronto-Sydney-San Francisco.Google Scholar
23.Kitajima, I, Kuriyama, M, Usuki, F, Izumo, S, Osarne, M, Suganuma, T, Murata, F, Nagamatsu, K (1989): Nasu-Hakola disease (membranous lipodystrophy). Clinical, histopathological and biochemical studies of three cases. J Neurol Sci 91: 3552.Google Scholar
24.Layde, PM, Erickson, D, Falek, A, McCarthy, BJ (1980): Congenital malformation in twins. Am J Hum Genet 32: 6978.Google Scholar
25.Little, J, Bryan, EM (1988): Congenital anomalies. In: MacGillivray, I, Campbell, DM, Thompson, B (eds): Twinning and Twins, p 207240. John Wiley & Sons, Chichester-New York-Brisbane-Toronto-Singapore.Google Scholar
26.Martin, NG, Robertson, DM, Chenevix-Trench, G, de Kretser, DM, Osborne, J, Burger, HG (1991): Elevation of follicular phase inhibin and luteinizing hormone levels in mothers of dizygotic twins suggests nonovarian control of human multiple ovulation. Fertil Steril 56 (3): 469474.CrossRefGoogle ScholarPubMed
27.McKusick, VA (1990): Mendelian inheritance in man. 9th ed. The Johns Hopkins University Press, Baltimore and London.Google Scholar
28.Nance, WE, Winter, PM, Segreti, WO, Corey, LA, Parisi-Prinzi, G, Parisi, P (1978): A search for evidence of heredity superfetation in man. In: Nance, WE, Allen, G, Parisi, P (eds): Twin Research: Biology and Epidemiology, p 6570. Alan R Liss, New York.Google Scholar
29.Nasu, T (1980): Pathology of membranous lipodystrophy. Asian Med J 23: 701726.Google Scholar
30.Nevanlinna, HR (1972): The Finnish population structure. A genetic and genealogical study. Hereditas 71: 195236.Google ScholarPubMed
31.Parisi, P, Gatti, M, Prinzi, G, Caperna, G (1983): Familial incidence of twinning. Nature 304: 626628.Google Scholar
32.Pierre Marie, M (1893): Mamelon surnuméraire transmis héréditairement dans une famille; coincidence avec plusieurs grossesses gémellaires. Réversion atavique A – ou création d'un type polymaste et polygène (?). Bull Soc Med Hosp Paris 10: 457459.Google Scholar
33.Rhine, SA, Nance, WE (1976): Familial twinning: a case for superfetation in man. Acta Genet Med Gemellol 25: 6669.Google Scholar
34.Richards, CS, Watkins, SC, Hoffman, EP, Schneider, NR, Milsark, TW, Katz, KS, Cook, JD, et al (1990): Skewed X inactivation in a female MZ twin results in Duchenne muscular dystrophy. Am J Hum Genet 46: 672681.Google Scholar
35.Sherman, SL, Turner, G, Sheffield, L, Laing, S, Robinson, H (1988): Investigation of the twinning rate in families with the fragile X syndrome. Am J Genet 30: 625631.CrossRefGoogle ScholarPubMed
36.Terayama, K (1961): Two cases of cystic bone disease showing peculiar features. J Jap Orthop Ass 35: 626 (in Japanese).Google Scholar
37.Veenema, H (1989): Clinical, cytogenetic and molecular aspects of the fragile-X syndrome. Thesis, University of Leiden: 1157.Google Scholar
38.Warkany, J (1971): Congenital malformations, p 12391247. Year Book Medical Publishers Inc., Chicago.Google Scholar