Literature DB >> 3221241

Familial motor neuron disease: differing penetrance in large pedigrees.

D B Williams1, D A Floate, J Leicester.   

Abstract

It is likely that adult-onset motor neuron disease is inherited more frequently than has previously been believed. We have studied 9 families with familial motor neuron disease and have found apparently wide variation in penetrance. Only one has autosomal dominant inheritance with high penetrance and in this family the average age of onset is similar to that reported in reviews of familial motor neuron disease. The remaining families have a pattern consistent with autosomal dominant inheritance with diminished penetrance. The average ages of onset in these families are comparable with those in sporadic motor neuron disease. Low penetrance appears to be related to higher average age of disease onset because gene carriers have an increased likelihood of dying from other causes before developing motor neuron disease. When penetrance is low the family history may be unknown, causing affected individuals to be mistakenly regarded as having sporadic disease. We conclude that the incidence of familial motor neuron disease is likely to have been underestimated by the exclusion of apparently sporadic cases in which the familial disease has low penetrance. These results and conclusions imply that the lower average age of disease onset reported in familial motor neuron disease may be due to selective recognition of high penetrance families with lower average ages of onset.

Entities:  

Mesh:

Year:  1988        PMID: 3221241     DOI: 10.1016/0022-510x(88)90100-1

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


  7 in total

1.  Familial adult amyotrophic lateral sclerosis: report of cases.

Authors:  M Maurelli; E Marchioni; D Bosone; S Boni; W Bolzani; R Cerretano; F Simonetti; F Savoldi
Journal:  Ital J Neurol Sci       Date:  1992-02

Review 2.  Clinical genetics of amyotrophic lateral sclerosis: what do we really know?

Authors:  Peter M Andersen; Ammar Al-Chalabi
Journal:  Nat Rev Neurol       Date:  2011-10-11       Impact factor: 42.937

Review 3.  British motor neuron disease twin study.

Authors:  A J Graham; A M Macdonald; C H Hawkes
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-06       Impact factor: 10.154

4.  Amyotrophic lateral sclerosis: update and new developments.

Authors:  Ashley J Pratt; Elizabeth D Getzoff; J Jefferson P Perry
Journal:  Degener Neurol Neuromuscul Dis       Date:  2012-02

Review 5.  Current pathways for epidemiological research in amyotrophic lateral sclerosis.

Authors:  Pam Factor-Litvak; Ammar Al-Chalabi; Alberto Ascherio; Walter Bradley; Adriano Chío; Ralph Garruto; Orla Hardiman; Freya Kamel; Edward Kasarskis; Ann McKee; Imaharu Nakano; Lorene M Nelson; Andrew Eisen
Journal:  Amyotroph Lateral Scler Frontotemporal Degener       Date:  2013-05       Impact factor: 4.092

6.  Lower motor neuron degeneration and familial predisposition to colonic neoplasia in two adult siblings.

Authors:  P J Shaw; P G Ince; J Slade; J Burn; N E Cartlidge
Journal:  J Neurol Neurosurg Psychiatry       Date:  1991-11       Impact factor: 10.154

7.  Motor neuron disease and multiple sclerosis among immigrants to England from the Indian subcontinent, the Caribbean, and east and west Africa.

Authors:  M Elian; G Dean
Journal:  J Neurol Neurosurg Psychiatry       Date:  1993-05       Impact factor: 10.154

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.