Literature DB >> 413703

Urgent opportunistic observations: the study of changing, transient and disappearing phenomena of medical interest in disrupted primitive human communities.

D C Gajdusek.   

Abstract

Two newly identified foci of usually rare disease occurring in high incidence in isolated primitive populations of West New Guinea are discussed as examples of medical problems that demand immediate intensive investigation because the unique naturally occurring experiments they represent are soon likely to be altered. These are: (1) amyotrophic lateral sclerosis, Parkinsonism, and dementia syndromes in a small population of Auyu and Jakai peoples in the Lowlands, and (2) an epidemic of burns from cysticercosis epilepsy from newly introduced Taenia solium in pigs in the Ekari people of the Wissel Lakes in the Highlands. A third new example is a focus of male pseudohermaphroditism among the Simbari Anga in the Highlands of Papua New Guinea. These are presented along with a series of eleven further examples of the kind of problems that require urgent opportunistic observation because of the extreme changes that investigation and therapeutic and preventive efforts themselves, as well as the inevitable effects of acculturation, will evoke from the moment an investigator or other outsider from a technologically advanced culture enters the previously isolated community.

Entities:  

Mesh:

Year:  1977        PMID: 413703     DOI: 10.1002/9780470715406.ch5

Source DB:  PubMed          Journal:  Ciba Found Symp        ISSN: 0300-5208


  9 in total

1.  Adult onset motor neuron disease: worldwide mortality, incidence and distribution since 1950.

Authors:  A M Chancellor; C P Warlow
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-12       Impact factor: 10.154

2.  The Scottish Motor Neuron Disease Register: a prospective study of adult onset motor neuron disease in Scotland. Methodology, demography and clinical features of incident cases in 1989.

Authors: 
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-07       Impact factor: 10.154

3.  Inherited and somatic mitochondrial DNA mutations in Guam amyotrophic lateral sclerosis and parkinsonism-dementia.

Authors:  Dana M Reiff; Rita Spathis; Chim W Chan; Miguel G Vilar; Krithivasan Sankaranarayanan; Daniel Lynch; Emily Ehrlich; Samantha Kerath; Risana Chowdhury; Leah Robinowitz; J Koji Lum; Ralph M Garruto
Journal:  Neurol Sci       Date:  2011-08-06       Impact factor: 3.307

4.  The Sambia "turnim-man": sociocultural and clinical aspects of gender formation in male pseudohermaphrodites with 5-alpha-reductase deficiency in Papua New Guinea.

Authors:  G H Herdt; J Davidson
Journal:  Arch Sex Behav       Date:  1988-02

Review 5.  The effect of 5α-reductase-2 deficiency on human fertility.

Authors:  Hey-Joo Kang; Julianne Imperato-McGinley; Yuan-Shan Zhu; Zev Rosenwaks
Journal:  Fertil Steril       Date:  2014-01-08       Impact factor: 7.329

6.  Utility of Scottish morbidity and mortality data for epidemiological studies of motor neuron disease.

Authors:  A M Chancellor; R J Swingler; H Fraser; J A Clarke; C P Warlow
Journal:  J Epidemiol Community Health       Date:  1993-04       Impact factor: 3.710

Review 7.  Kuru: a journey back in time from papua new Guinea to the neanderthals' extinction.

Authors:  Pawel P Liberski
Journal:  Pathogens       Date:  2013-07-18

Review 8.  Kuru, the First Human Prion Disease.

Authors:  Paweł P Liberski; Agata Gajos; Beata Sikorska; Shirley Lindenbaum
Journal:  Viruses       Date:  2019-03-07       Impact factor: 5.048

9.  Disease concepts and treatment by tribal healers of an Amazonian forest culture.

Authors:  Christopher N Herndon; Melvin Uiterloo; Amasina Uremaru; Mark J Plotkin; Gwendolyn Emanuels-Smith; Jeetendra Jitan
Journal:  J Ethnobiol Ethnomed       Date:  2009-10-12       Impact factor: 2.733

  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.