The Gist of Genetics Disorders in Children

Sufyan Abid Dogra*

Published Date: 2021-12-28

Sufyan Abid Dogra*

Department of Psychiatry, Bradford Institute for Health Research, United Kingdom

*Corresponding Author:
Sufyan Abid Dogra Department of Psychiatry, Bradford Institute for Health Research, United Kingdom, Email :Sufyan.Dogra@bthft.nhs.uk

Received: December 01, 2021; Accepted: December 15, 2021; Published: December 22, 2021

Citation: Dogra SA (2021) The Gist of Genetics Disorders in Children. J Child Dev Disord.7 No.12. e001

Visit for more related articles at Journal of Childhood & Developmental Disorders

Genetics is a genetic study. Our genes carry information that is passed on from one generation to the next. For example, genes are responsible for children with blonde hair, such as mothers, while siblings have brown hair, just like their father. The gene also determines why certain diseases occur in the family and whether the child is male or female. Genetic disorders occur when one or more genes have a problem with their code, causing health problems. Genetic diseases can occur when a child inherits from one or both parents. In some cases, it is rare in a child (and parents do not have a genetic predisposition).

To form an embryo, an egg from the mother and sperm from the father come together. Egg and sperm all have 1/2 of a strong and fast chromosome. The egg and sperm together bring the baby a whole set of chromosomes. That way we can inherit a few stories from our mother and a few from our father. Angelman Syndrome is a condition in which a person is characterized by severe mental retardation, short stature, inability to speak, strong arm movements, and a restless step. Deficiency of biotinidase deficiency of the enzyme biotinidase is a symptom of this genetic disorder. This enzyme is needed for biotin, vitamin B, to be digested. Congenital malformations (birth defects) are health problems or abnormal physical changes that occur when a baby is born. Carpenter Syndrome is a very rare congenital condition (present at birth) in which the baby's forearm, fingers, and toes grow abnormally. Genetics and chromosomes are disrupted, depleted, or have additional components. This can lead to serious baby health problems and birth defects.

Before and during pregnancy you can be tested to see if your baby is at risk for a specific genetic problem or birth defect. A genetic counselor can help you understand the results of tests and how genetics, birth defects, and other medical conditions are passed on to your family. Your family health history can help you, your health care professional, and your genetic counselor in diagnosing a genetic disorder that affects your family. Genetics are part of genetics. They contain instructions for making DNA, proteins. Proteins do a lot of work within a cell. They move cells from one place to another, build structures, detoxify, and perform many other repair tasks. Sometimes there are genetic mutations, mutations in one or more genes. Genetic modification alters genetic instructions for protein synthesis, causing them to malfunction or fail to function properly. This can lead to a condition called hereditary disorder. Genetics are part of the gene. They are passed on from parents to their children. They contain instructions for making DNA, proteins. Proteins do a lot of work in a cell. They move cells from one place to another, build structures, detoxify, and perform many other repair tasks. Sometimes there are genetic mutations, mutations in one or more genes. Genetic modification alters genetic instructions for protein synthesis, causing them to malfunction or fail to function properly. This can lead to a condition called genetic disorder.

 

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