Which of the Following Is a Genetic Disorder

Phenylketonuria is a genetic disorder of. C Whole chromosome extra missing or both see chromosome abnormality T Trinucleotide repeat disorders.

In This Biology Topic We Will Cover The Following Ausvels Science Understanding Biological Sciences Achievement St Genetic Disorders Science Biology Biology

The counselors evaluate the results of the tests.

. Gene is extended in length. Albinism is a rare group of genetic disorders that cause the skin hair or eyes to have little or no color. At birth infants are tested for the genetic disorder.

PKU is caused by an enzyme deficiency in which. 3 Irritable Bowi Syndrome IBS 4 Sickle cell Anaemia. A person with Huntingtons disease will pass the disease on to 100 percent of their children.

It may also occur later in life. Genetic mutations that affect the production of a pigment called melanin. Which of the following is true.

Resulting from a variation in the genetic pattern. The counselors check the family medical history and medical records of parents to estimate the chances of inheritance of genetic disorder or disease in a developing fetus. A genetic disorder is a disease caused in whole or in part by a change in the DNA sequence away from the normal sequence.

All of the choices are correct O Phenylketonuria PKU Cystic Fibrosis O Sickle Cell Anemia. O phenylketonuria PKU O kwashiorkor cystic fibrosis O hyperchloremic acidosis. The genetic counseling will involve the following steps.

Also found in people with immune disorders it occurs most commonly because of decreased intake or absorption of vitamin A. Which of the following genetic disorders is caused by an autosomal dominant allele. Leukaemia is the blood cancer caused by the effect of some mutagen.

Haemophilia is a sex-linked recessive disease. Asked Jul 17 2021 in Biology by somi_98 210k points 0 like 0 dislike. Cell membrane Question 57 1 pts Which of the following is a genetic.

The correct response is C because polycystic kidney disease is an example of an autosomal dominant disease because the gene carrying the mutation is located on one of the autosomes of the affected parent and the affected person has a 50 chance of passing the abnormal gene to each of the children. Correct option is D Scurvy is the disease caused by the deficiency of Vitamin C. Which of the following statements is true of autosomal recessive disordersAs part of an orientation to a genetic counseling practice a group of medical students is differentiating between autosomal recessive disorders and autosomal dominant disorders.

Which of the following is not a genetic disorder. This genetic mutation is not present in either parent only the offspring. Which one of the following is not a genetic disease.

1 answer 22 views. Give the evidence from the analysis which suggests that the disease is sex-linked and caused by a recessive allele. Haemophilia is a genetic disorder in which the body unable to form blood clots.

Genetic disorders can be caused by a mutation in one gene monogenic disorder by mutations in multiple genes multifactorial inheritance disorder by a combination of gene mutations and environmental factors or by damage to. A Tay Sachs disease b Sickle cell disease c Huntingtons disease d Cystic fibrosis. In___ a missing enzyme causes lipid molecules to accumulate in the brain.

Sickle -cell anaemia is a genetic disorder The cause of the disease is due to. Goiter is the disease caused by the deficiency of Iodine that hinders the functioning of the thyroid gland. Which of the following is a genetic disease caused by a gene described as autosomal recessive.

The subsitution of glutamic acid in place of aspartic acid The substi. Asked1 dayagoin Biologyby Somyakumari120kpoints class-12. Asked Jun 17 2021 in Biology by riyapreprise 453k points 0 like 0 dislike.

Which one of the following is not genetic disease. 1 answer 24 views. Xerophthalmia is a serve drying of the eye surface caused by a malfunction of the tear glands.

A genetic disorder is caused by a condition. A cherry red spot which can be a feature of several storage disorders including TaySachs disease. Albinism is also associated with vision problems.

A child who inherits one copy of the gene that causes Huntingtons is a carrier for the disease. Multifactorial genetic inheritance disorders. Which of the following genetic diseases is caused by a dominant gene.

Xerophthalmia is not a genetic disorder. Irritable Bowi Syndrome IBS b. Huntingtons disease is a genetic disorder that is caused by a dominant allele.

Sickle cell anemia b. Which of the following is a genetic disorder resulting in defective assembly of a chloride transport protein and characterized by severe respiratory and digestive distress. Dup - Duplication of a gene or genes.

A genetic mutationalteration that appears for the first time in a family as a result of a variant in an egg or sperm cell of the parents or a variant that occurs in the fertilized egg itself. Biology questions and answers. Symptoms include night blindness and eye irritation.

This is called a de novo De novo genetic mutation. Amino acids build up in the brain. Study the pedigree analysis given showing the inheritance of the disease in a family and answer the questions that follow.

Mitochondrial genetic inheritance disorders. The counselors order genetic testing.

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