Thesis Abstract

Abstract
The study aimed to investigate the causal relationship between advanced maternal age and Down syndrome in the Busa Buji community located in Jos North, Plateau State. Down syndrome is a genetic disorder caused by the presence of an extra copy of chromosome 21. Advanced maternal age, typically considered as 35 years and older, has been identified as a significant risk factor for Down syndrome due to the increased likelihood of chromosomal abnormalities during maternal meiosis. A mixed-methods approach was employed for data collection, including quantitative analysis of medical records from healthcare facilities in the community and qualitative interviews with mothers of children with Down syndrome. The quantitative analysis focused on identifying the prevalence of Down syndrome cases among mothers of advanced maternal age compared to younger mothers. Additionally, the study explored the specific chromosomal abnormalities associated with Down syndrome in the study population. Preliminary findings from the quantitative analysis revealed a higher prevalence of Down syndrome cases among mothers of advanced maternal age in the Busa Buji community. The data indicated a statistically significant association between advanced maternal age and the likelihood of having a child with Down syndrome. Furthermore, the qualitative interviews provided insights into the experiences and challenges faced by mothers raising children with Down syndrome in the community. The study findings have important implications for healthcare providers and policymakers in addressing the impact of advanced maternal age on Down syndrome prevalence in the Busa Buji community. By understanding the causal relationship between advanced maternal age and Down syndrome, targeted interventions and support services can be developed to assist families affected by this genetic disorder. In conclusion, this research contributes to the existing literature by providing empirical evidence of the causal relationship between advanced maternal age and Down syndrome in the Busa Buji community. The findings underscore the importance of early prenatal screening and genetic counseling for mothers of advanced maternal age to better understand and manage the risks associated with chromosomal abnormalities leading to Down syndrome.

Thesis Overview

1.0       INTRODUCTION

1.1       BACKGROUND OF STUDY

Down syndrome is a genetic disorder caused when abnormal cell division results in an extra chromosome 21.

This genetic disorder, which varies in severities cause lifelong intellectual disability and developmental delays and in some people it causes health problems.

Down syndrome is the most common genetic chromosomal disorder and cause of learning disabilities in children.

Better understanding of Down syndrome and early intervention can greatly increase the quality of life for children and adults with the disorder and help them live fulfilling lives; although it has no cure (Mayo Clinic, April 19, 2014).

This syndrome took its name from John Langdon Down, an English physician who in the late 19th century was able to publish an accurate description of a person with this syndrome hence the name Down syndrome.

There are certain characteristics associated with this syndrome such as:

·               Low muscle tone

·               Small stature

·               An upward slant to the eyes

·               A single deep crease across the centre of the palm

·               Flattened facial profile

·               Heart problem

·               Respiratory problems among others.

It is more than 75 years now, since maternal age effect in Down syndrome was discovered and 50 years since the genetic background in Down syndrome involving an extra chromosome 21 material was identified.

Down syndrome is a genetic syndrome occurring in from 1 in 650 to 1 in 1000 live births. In 95% of cases, Down syndrome is caused by non-disjunction during cell division, with mothers contributing the extra chromosome in 85% cases. When this disjunction occurs after fertilization it leads to Down syndrome where one line of cells in the developing fetus contains an extra copy of chromosome 21 and the second line of cells in the developing fetus does not.

Risk for Down syndrome is associated with maternal age. Children with Down syndrome are impaired in verbal processing and expressive language (Fidler, 2008).

In recent years between the 19th century and the 20th century the number of babies born with Down syndrome increased about 30%. Older mothers are likely to have babies affected by Down syndrome than younger mothers. In other words the prevalence of Down syndrome increases as the mother’s age increases.

The actual cause of this syndrome is idiopathic although, maternal age and paternal age are factors that have been linked to an increased chance of having a baby with this syndrome. However due to higher birth rates in younger women which could also be a predisposing factor, 80% of children with Down syndrome are born to women who are advanced in age.

The additional partial or full extra chromosome 21 can originate either from the mother or father. Approximately 5% of cases have been traced to the father. Down syndrome is no respecter of race or economy.

In Down syndrome,only 1% of all cases occur as a result of translocation (hereditary) it occurs sporadically and maternal age cannot be linked to the risk of translocation.

The risk of a mother having a baby with Down syndrome rises dramatically after she reaches 35 years of age.

A woman is born with all of the eggs (ova) she will ovulate with for the rest of her life. So if one is 30 years when one conceives, then the egg (ova) one conceived with is also 30 years old; this is applicable to all age group over 35 years. As the eggs (ova) age, the more likely they are to have errors that can result in trisomies including trisomy 21 (Down syndrome) (Kathleen, 2016).

Advanced maternal age is a risk factor for Down syndrome. This risk factor reaches 3.6% of live births when mother’s age is around 44 years. It cannot be prevented but can be detected before the child is born.

A woman’s chance of giving birth to a child with Down syndrome increases with age because older eggs (ova) have a greater risk of improper chromosome division (Mayo Clinic, 2014).

As a woman ages, her fertility that is, the chance she will get pregnant is reduced. On average, this decline begins slowly in the early thirties and speeds up in the late thirties and forties (Rowe, 2008).

1.2       STATEMENT OF PROBLEM

The researcher observed that more often than not, more children are coming down with trisomy 21, especially to mothers who are elderly (advanced in age).However, ignorance tends to play a major role. Hence the researcher wants to investigate on the relationship between advanced maternal age and Down syndrome and the possible ways of creating awareness because this syndrome predisposes babies born to advanced mothers to numerous pathological disorders.

1.3       RESEARCH QUESTIONS

·       How knowledgeable are the residents of Busa Buji community about Down syndrome?

·       How knowledgeable are the residents of Busa Buji community about the causes of Down syndrome?

·       What is the prevalence rate of Down syndrome?

·       What is the best means of disseminating information on the cause of Down syndrome?

·       What are the ways of enforcing early and curtailed child bearing?

1.4       OBJECTIVES OF STUDY

The main objective of this study is to determine the causal relationship between advanced maternal age and Down syndrome in Busa Buji community, Jos North, plateau state.

The main objectives will be achieved through the following specific objectives which include:

·       To assess the level of knowledge of the residents of Busa Buji community on Down syndrome.

·       To determine the level of knowledge/ awareness of the residents of Busa  Buji street on the cause of Down syndrome .

·       To determine the prevalence rate of Down syndrome.

·       To educate the residents of Busa Buji community to gain full knowledge of Down syndrome and its relationship to advanced maternal age.

·       To enforce the need for early and curtailed child bearing.

1.5       SIGNIFICANCE OF STUDY

To heighten the awareness of health planners in the community that have for a long time considered haemoglobinopathies to be the major genetic disorder and that Down syndrome is also a major genetic disorder. In order to prepare the ground for prevent measures which will provide a baseline for further research work.

This will create awareness to all ambitious ladies n Busa Buji community, Jos, North, Plateau state; that while pursuing education to the highest level as well as other things, child bearing should be put into consideration while one is not yet advanced in age.

1.6       SCOPE OF STUDY

This study is focused mainly on 100 respondents in Busa Buji community, Jos North, Plateau state on the Reationship between Advanced Maternal Age and Down Syndrome.

1.7       OPERATIONAL TERMS

Advanced Maternal Age

A term used to describe pregnant woman over age 35 years.

Alzheimer’s Disease

Progressive degenerative disease of the brain that leads to dementia, (loss of intellectual abilities)

Brush Field Spots

Little white spots that are slightly arranged in a ring concentric with the pupils.

Chromosome

A carrier of genetic information.

Genetic

Having to do with genes which are the basic biological unit of hereditary.

Hypotonia

Decreased muscle tone and strength that results in floppiness.

Incedence