If a child has an autosomal dominant disorder, what can be concluded about the parents? Explain please

Q: Differentiate congenital from genetic defects.

A: Genes are generally referred to as the basic unit of heredity. They are a part of DNA, and are…

Q: Explain the Autosomal Recessive Disorders ?

A: Genetics is a part of science worried about the investigation of genes, genetic variety, and…

Q: O Autosomal Dominant

A:

Q: Explain tyrosinemia .

A: Amino acids are the components of proteins. Individual amino acids undergoes metabolism, which…

Q: A. Identify a substance or chemical in a certain product that could trigger a genetic disorder. B.…

A: The hereditary ingredient is usually defined as the term that stated that the cell is the genetic…

Q: Define the Autosomal Dominant Disorders ?

A: Answer: Introduction: Inheritance means the transfer of genetic data is from parent to child.

Q: A man and woman are both affected by an autosomal dominant disorder, polydactly. Their first child…

A: The alleles are the alternative forms of a gene that are located on the same locus of a homologous…

Q: suspected

A: Abstract  Past research demonstrates a phenotypic relationship between childhood mal treatment and…

Q: Define dystrophies

A: Answer: Introduction: Presently no cure for muscular dystrophy (MD), but a diversity of treatments…

Q: Which of the following can be identified by anabnormal karyotype?a. Sickle cell diseaseb. Cystic…

A: Cytogenetics is a field of study that focuses on the chromosomes and associated disorders caused by…

Q: In autosomal dominant disorders, the recurrence risk is ¾(75%) when one affected parent and one…

A: When a child receives one version of a mutant gene from one parent, autosomal dominant inheritance…

Q: Match the Disorder to its description for numbers 11-15:

A: Any disorder of the nervous system leads to a neurological disorder. Any structural, electrical or…

Q: What autosomal dominant and What is an example of an autosomal dominant disorder?

A: The inheritance patterns explains how a disease is transmitted in families. These patterns help to…

Q: Explain what acquired genetic abnormalities (after birth)  are and why (almost always) they are not…

A: Genetic abnormality refers to the change in the genetic makeup of an individual due to various…

Q: Huntington’s disease is a dominant disorder. Suppose that Kent and Alice are both heterozygous for…

A: Huntington's disease [HD] is a brain disorder. This disease is caused by the defective gene present…

Q: Explain the nondisjunction event that would cause a Turneror Klinefelter syndrome individual.

A: Nondisjunction refers to the failure of homologus chromosomes or sister chromatid to separate during…

Q: Why is autosomal Monosomy lethal?

A: Most living species have DNA as their genetic material. It is the cell's information centre,…

Q: Mention any two autosomal genetic disorders with their symptoms.

A: Introduction The two autosomal genetic disorders with their symptoms are as follows.

Q: Describe the causes of down syndrome. Explain in a detailed manner.

A: Down syndrome is a genetic disorder that is mainly caused by the chromosomal abnormalities during…

Q: List two examples of sex-linked disorders.

A: Sex-related disorders, also called sex-linked diseases are inherited by one of the X or Y…

Q: If both parents have an autosomal dominant trait, what can you say about their children? Explain

A: Autosomal dominance is a pattern of inheritance character of some genetic dis order. Autosomal…

Q: Prepare a chart that identifies the characteristic features of the following disorders: Down…

A: Introduction- Down syndrome is genetic chromosomal congenital abnormality resulting from trisomy of…

Q: What is the life expectancy of someone with Turner's syndrome?

A: Turner's syndrome is an example of Aneuploidy. Fertilization of an egg X by a sperm O produces an…

Q: What pattern does the genetic disorder follow

A: Introduction Sickle cell anaemia is a type of sickle cell illness that is passed down the…

Q: Describe two potential problems resulting frombleeding.

A: A bleeding disorder is a medical condition that creates a problem with the clotting of blood. After…

Q: What is autosomal

A: Autosomes are those chromosomes that are not sex chromosomes, humans have 22 pairs of autosomes and…

Q: Identify a disorder caused by a chromosomal abnormality and how the disorder affects the individuals…

A: Chromosomal abnormality are one of the main reasons for many inherited disorders and traits, and…

Q: What is a monogenic disease?

A: A monogenic disease is a disease that results from a flaw is a single gene that is the direct cause…

Q: Identify and describe the major events during the fetal stage ofdevelopment.

A: The fusion of an ovum and a sperm produce a zygote. This process is called fertilization. After…

Q: Explain autosomal dominant and recessive traits.

A: Any genetically determined characteristic of living things that could be passed on to their…

Q: Identify changes in physiological and psychosocial function associated withimmobility ?

A: A state in which an individual is not able to do the purposeful physical movement of the complete…

Q: A disorder that only ever appears in males and is present in all male children is a(n) ________.…

A: Y linkage, also known as holandric inheritance, refers to the inheritance of features from genes on…

Q: If a condition is a “genetic" disorder, what does that mean and how would it be different from a non…

A: A genetic condition occurs when you inherit an altered (changed) gene from your parents that…

Q: Give some examples for down syndrome

A: Genes are housed in chromosomes, which are structures. Numerical or structural chromosomal…

Q: What is the  cause of  Miller syndrome?

A: Miller syndrome or postaxial acrofacial dysostosis is a rare condition that affects the development…

Q: Define congenital, genetic, chromosomal, developmental,and multifactorial disorders.

A: Chromosomal abnormalities are uncommon on their own, but they are prevalent in groups, whereas…

Q: What is a hiploid

A: Meiosis is cell division where diploid chromosomes divided to give rise to a haploid number of…

Q: Define polygenic

A: A trait is any feature of an organism, such as eye color. A phenotype is the set of an organism’s…

Q: what are the types of down syndrome

A: Down syndrome is a condition in which a person has an extra chromosome. people with Down syndrome…

Q: Present clinical consequences of most commonly identified numerical chromosome abnormalities.

A: Chromosomes are thread like structures which are found in the nucleus of the eukaryotic cells. In…

Q: What would be the phenotypes for each of the following genotypes for Huntington’s Disease? a.  Hh =…

A: Neurodegenerative diseases are a diverse group of disorders. They have a progressive degeneration…

Q: What is the most likely mode of transmission of the trait? autosomal dominant

A: Mode of Inheritance predicted by Pedigree -- A pedigree represent family members and relationships…

Q: Describe the cause and effect of Down syndrome.

A: Introduction:- genetic chromosome 21 disorder causing developmental and intellectual delays. Down's…

Q: Explain about familial hypercholesterolemia ?

A: Introduction:' Cholesterol is the significant sterol present in the cell membrane of an animal cell.…

Q: Define incomplete dominance. Describe autosomal dominant and autosomal recessive disorder with ONE…

A: INCOMPLETE DOMINANCE When neither of the alleles are dominant then incomplete dominance is said to…

Q: Differentiate a multifactorial disorder from a chromosomal disorder.

A: Multifactorial diseases are not confined and do not follow any specific pattern of single gene…

Inheritance and Mendelian Genetics

Inheritance means the passing of traits to offspring from parents. These traits could be passed either through asexual reproduction or sexual reproduction. The offspring receives the genetic material from the parents. Mendelian inheritance is a certain biological inheritance that follows the rules and principles laid down by Gregor Mendel in 1865. The initial hypothesis was considered wrong, but other inheritance theories modified the concept of inheritance and thus genetics.