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Heredity and Polyposis Coli J. Utsunomiya 1 12nd. Dept. of Surgery, Tokyo Medical and Dental University pp.1149-1156
Published Date 1974/9/25
DOI https://doi.org/10.11477/mf.1403111859
  • Abstract
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Central registration system

 An attempt has been made to establish a central registration system for familial polyposis coli (FPC), which is defined as a so-called hereditary disease characterized by multiple adenomas deffusely distributed throughout the colon and rectum. The central registration system on this disease have been established. Information on the proband has been collected through random inquiries at hospitals, by questionaires on the cases published in clinical journals or in pathological autopy records, from the patients visiting us and from the physician's voluntary reports. Information on 205 cases belonging to 165 families has been collected at present and 37% of them are found to be published officially in the journals. The individuals are identified and their exact “Working pedigrees” are constructed covering at least 4th grade of consanquinity by means of reviewing the official family register record (Koseki) and the information on the affected relatives is being collected by communicating with the families of the patients and/or by reviewing the death certificates. The accumulated information is computerized for permanent preservation and analysis.

 During these operations, linkage of independently registered pedigree has been infrequently observed. While the linkage occurs on the same generation level (“horizontal linkage”), it could also occur on the different levels (“vertical linkage”) as in a pedigree in which one of the antecedents of the propositus was found to have appeared in literature as an independent pedigree 40 years ago. Follow-up survey : In the initial inquiry group, we found newly affected cases six families during the following seven years. This happened in two families in which the disease had not been confirmed at the previous suvery in other than the propositi, so-called sporadic or non-familial case.

 We actually confirmed more than 459 persons affected at present or in the past and were able to locate about 1,164 possible polyposis carriers requiring examination.

Expression of the trait

 The age of onset of the initial symptom is considerably earlier in female (24.7 years en the average) than in male (31.6).

 The earliest manifestation of the trait that we experienced was a single polyp detected in a girl of 8 years of age. The polyps are considered to increase in number with age. We have observed these over middle age with segmental distribution of polyps who were a member of typical FPC. Our study revealed that the “expressibility” of the colonic polyps is considerably different individuals as well as among the families, Veale's observation on juvenile polyposis in the family of FPC is considered as a phenomenon of “specificity”.

 As extracolic lesions, gastric polyps are detected in 66%. Any one of Gardner's stigmated is detected in 35.7% of personal cases (incomplete type of FPC) while typical stigmata are associated in 7.1% (complete Gardnertype) and no stigmata are detected in 57.1% (simple FPC).

 These data are considerably higher than those faund in survey group and indicate that FPC principally has the characteristics of producing dwerse types of extracolic neoplastic lesions, The reason for the existence of Gardner's syndrome could be explained by different grade of expressivility of “pleiotrophyic phenomenon”. Penetrance is calculated as 0.679.

Familial case and Non-familial case

 After intensive family and follow up survey incidence of familial cases has been increased currently up to 0.52. However, there remained still 0.48 of non-familial cases. Our current data on relative fitness are 0.88. This produced 0.12 selection coefficient. This value showed still large discrepancy in the value of mutation coefficiency (0.41) calculated by us. Existence of phenocopy is not entirely neglected.

Mode of inheritance

 Male to female ratio is 1 : 0.6; this is considered as “sex controlled effect”. Our analysis suggests that female individual carring the gene may be lost in early stage after birth as well as in utero for some reason. Segregation ratio is 0.377; this is modified by penetrance (0.68) to produce 0.554.


Copyright © 1974, Igaku-Shoin Ltd. All rights reserved.

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電子版ISSN 1882-1219 印刷版ISSN 0536-2180 医学書院

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