Endogamous groups in Western India have been known to have a wide degree of genetic diversity. Analysis of the data available on some of the endogamous groups belonging to two main communities attending the Tata Memorial Hospital, Bombay, viz. Hindus from Maharashtra, and Hindus from Gujarat show that one of the endogamous groups, the Maharashtrian Brahmin has a significantly different pattern of cancer site distribution compared to the other groups studied. Maharashtrian Brahmins have a low relative frequency of cancer of the oral cavity and high relative frequencies of cancer of the oropharynx and cancer of the oesophagus. The tobacco chewing habit pattern seems to have a bearing on the proportion of cancer of the oral cavity observed in the groups studied. However, in the case of cancer of the oropharynx and cancer of the oesophagus, factors besides smoking and chewing habits seem to be playing a role. A further study is indicated to clarify the points raised by the study.
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http://dx.doi.org/10.1038/bjc.1971.77 | DOI Listing |
Orphanet J Rare Dis
August 2024
FRIGE Institute of Human Genetics, FRIGE House, Ahmedabad, India.
BMC Neurol
July 2024
Faculty of Medicine, University of Porto, Porto, Portugal.
Introduction: The high prevalence of endogamy, or inbreeding, in northeastern Brazil, is due to historical and cultural factors, with large families living in cities far from the coast and subject to low socioeconomic and infrastructure levels. This breeding practice results in low genetic variability with an increased prevalence of rare autosomal recessive and neurodegenerative diseases, such as spinal muscular atrophy (SMA).
Objective: Understanding the impact of communicating the diagnosis of SMA on the mental health of patients and their families and the differences between the Northeast (endogamous region) and the other regions of Brazil (non-endogamous ones).
Biochem Genet
July 2024
Department of Anthropology, Dr. Harisingh Gour Vishwavidyalaya (A Central University), Sagar, Madhya Pradesh, 470003, India.
Located on India's eastern coast, Odisha is known for its diverse tribes and castes. In the early days of genome sequencing technology, researchers primarily studied the Austroasiatic communities inhabiting this region to reconstruct the ancient origins and dispersal of this broad linguistic group. However, current research has shifted towards identifying population and individual-specific genome variation for forensic applications.
View Article and Find Full Text PDFNeurogenetics
October 2024
Genomics and Molecular Medicine, CSIR-Institute of Genomics and Integrative Biology, Mall road, New Delhi, 110007, India.
Background: The ethnic diversity of India provides a unique opportunity to study the history of the origin of mutations of genetic disorders. Spinocerebellar ataxia type 27B (SCA27B), a recently identified dominantly inherited cerebellar disorder is caused by GAA-repeat expansions in intron 1 of Fibroblast Growth Factor 14 (FGF14). Predominantly reported in the European population, we aimed to screen this mutation and study the founder haplotype of SCA27B in Indian ataxia patients.
View Article and Find Full Text PDFEur J Popul
June 2024
Federal Institute for Population Research, Wiesbaden, Germany.
For the German context, we investigate whether the number of children ever born differs between mixed unions (exogamous unions between natives and migrants or migrant descendants) and endogamous unions (unions among co-ethnics). Our theoretical considerations are derived from assimilation theories, which view exogamous unions as indicators of assimilation processes, and the framework on migrant fertility. The migrant (or descendant) partner in an exogamous union may adapt to the majority group, both partners may adapt to each other, or both partners may constitute a selected group in their fertility preferences.
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