Results 11 to 20 of about 6,342 (247)

Consanguineous Marriages in Pakistan [PDF]

open access: yesThe Pakistan Development Review, 1994
In societies where marriage is nearly universal, and the fertility process is almost entirely through marital union, the factors associated with the occurrence of marriage, and through it the reproduction and rearing of children, need to be continuously assessed.
Mohammad Afzal   +2 more
openaire   +2 more sources

Histidinaemia in a consanguineous marriage [PDF]

open access: yesJournal of Medical Genetics, 1974
Support to the autosomal recessive inheritance for histidinaemia is given by the finding of an affected product from a first-cousin marriage. The histidine loading test done on the parents confirms previous reports that female heterozygous metabolize the amino acid at a slower rate than male heterozygous.
I, Rostenberg   +4 more
openaire   +2 more sources

Dental Anomalies in Consanguineous Marriage: A Clinical-Radiological Study

open access: yesInternational Dental Journal, 2022
Objective: This study aimed to evaluate nonsyndromic developmental dental anomalies (DDAs) in individuals born from consanguineous and nonconsanguineous marriages and the possible effects of these marriages on self-reported systemic diseases.
Nuray Bağcı   +3 more
doaj   +1 more source

Traditions matrimoniales dans la région de Rabat-Salé-Zemmour-Zaer au Maroc

open access: yesBulletins et Mémoires de la Société d’Anthropologie de Paris, 2007
The practice of consanguineous marriage has been widespread for hundreds of years, and is still very common, especially among various Middle Eastern, Asian and African populations where 20 to 50% + of marriages are consanguineous.
Hinde Hami   +2 more
doaj   +1 more source

Assessment of level of Awareness regarding Thalassemia Major among Parents of Affected Children

open access: yesJournal of Rawalpindi Medical College, 2021
Background: Thalassemia major is amongst the most common genetic disorders in developing countries like Pakistan. This research project aims to assess the level of knowledge among people related to thalassemia and the number of thalassemia cases linked ...
Faizan Fazal   +5 more
doaj   +1 more source

The association between consanguineous marriage and offspring with congenital hearing loss

open access: yesAnnals of Saudi Medicine, 2020
BACKGROUND: Consanguinity is a commonly recognized practice among marriages in the Middle East and may lead to an increase in the prevalence of inherited disorders. Autosomal recessive deafness is the most common form of inherited congenital hearing loss
Aljohara M. Almazroua   +4 more
doaj   +1 more source

Parental consanguinity increases the risk of congenital malformations

open access: yesRehman Journal of Health Sciences, 2021
Introduction: Congenital malformation is a physical or structural abnormality present either prenatally or after birth. These anomalies are either primary or secondary malformation.
Maheen Gul   +4 more
doaj   +1 more source

On the Adaptive Origins and Maladaptive Consequences of Human Inbreeding: Parasite Prevalence, Immune Functioning, and Consanguineous Marriage

open access: yesEvolutionary Psychology, 2010
We propose that consanguineous marriages arise adaptively in response to high parasite prevalence and function to maintain coadapted gene complexes and associated local adaptation that defend against local pathogens.
Ashley D. Hoben   +4 more
doaj   +1 more source

Infant death and consanguineous marriage [PDF]

open access: yesBMJ, 1994
EDITOR, - Perinatal mortality and infant mortality are important indicators of community health Consanguineous marriage increases the risk of having children with autosomal recessive disorders and may be a cause of perinatal and infant death that cannot be prevented.1,2 We recently compared perinatal and infant mortality in children with a Norwegian ...
K H, Orstavik, R, Lindemann, J, Steen
openaire   +2 more sources

Milestone Attainment in Young Children With Arthrogryposis Multiplex Congenita: Developmental Profile and Associated Factors

open access: yesAmerican Journal of Medical Genetics Part C: Seminars in Medical Genetics, EarlyView.
ABSTRACT Evidence on developmental milestones in children with arthrogryposis multiplex congenita (AMC) under the age of five is scarce. This multisite cross‐sectional study described developmental status and examined factors associated with milestone attainment in 143 children aged 0–66 months from a pediatric AMC Registry.
Ahlam Zidan   +13 more
wiley   +1 more source

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