A Genetic Study of Paget’s Disease (Osteitis Deformans) in Monozygotic Twin Brothers-Reference-Cited by-同舟云学术

A Genetic Study of Paget’s Disease (Osteitis Deformans) in Monozygotic Twin Brothers

Published:1952-01 Issue:1 Volume:1 Page:67-79
ISSN:1120-9623
Container-title:Acta geneticae medicae et gemellologiae
language:en
Short-container-title:Acta genet. med. gemellol.

Author:

Aschner Bertha M.,Hurst Lewis A.,Roizin Leon

Abstract

Observation of the behaviour of a pair of one-egg twins, incompletely concordant with resspect to Paget’s disease, is consistent with the courrent theory (based on 57 families in which the disease has occurred in more than one member of the family, and one other pair of one-egg twins), that the condition is of genetic origin, the gene responsible being an incompletely dominant autosomal gene with variable degrees of penetrance and expressivity.

Publisher

Cambridge University Press (CUP)

Reference38 articles.

1. Schwartz L. A. , Paget’s disease in three male siblings. J. Mich. Med. Soc. 47: 1244 (1948).

2. Martin E. , Considerations sur la maladie de Paget. Helvet. Acta Med. 14: 319 (1947).

3. Rast H. and Weber P. F. , Paget’s bone disease in three sisters. Brit. Med. J. 918 (1937).

4. Faugeron R. , Essai sur les Rapports de la Syphilis et de la Maladie Osseuse de Paget. Thèse de Paris (1923).

5. Eeden J. H. V. , Isolierte Pagetsche Krankheit des Schädels mit Stimhirnerscheinungen und Korsakoffschem Symptomenkomplex. Jahrb. Psychiat. 46: 53 (1928).

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