Q: What is the treatment for Turner syndrome?
A: Turner's syndrome is a chromosomal condition that affects the development of women. It results when…
Q: explain thigmotropism?
A: Thigmotropism means, moving with help of touch. Where, thigmo = touch, and tropism = tendency of an…
Q: Define about the Mutation and sickle cell disease ?
A: The genome consists of 1 to many long molecules of DNA, and mutation will occur probably anyplace on…
Q: Are the symptoms of wolf hirschhorn syndrome chronic or acute?
A: A deletion of genetic material at the end of chromosome 4's short (p) arm causes Wolf-Hirschhorn…
Q: What is Guillain-Barré syndrome (GBS) ?
A: Autoimmune disorder is a type of disorder in which our own system attacks our body mistaken it as a…
Q: Describe the phenotype for the following two diseases and name the gene linked to each disorder. a)…
A: Genetic disorders Genetic disorders are caused due to mutations in the gene of an individual. These…
Q: Describe both the primary gene or protein defect and the resulting phenotype for the following…
A: A)Cystic fibrosis is an autosomal recessive disease.It is a progressive disease and requires daily…
Q: How can wolf hirschhorn syndrome progress or change?
A: Many cases of Wolf-Hirschhorn syndrome (WHS) (about 50-60%) are not inherited from a parent and are…
Q: Explain the cause of Klinefelters syndrome. Give any four symptoms shown by sufferer of this…
A: Normally human have 22 pairs of autosomes and 1 pair of sexual chromosomes. Trisomy is a condition…
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: Define about Jacobs Syndrome ?
A: There are 2 types of chromosomes- autosomes and sex chromosomes. Sex chromosomes are responsible…
Q: Explain the Impaired Mitochondrial Function ?
A: Cells are the smallest functional and structural unit of all organisms. All cells have a plasma or…
Q: What causes Turner syndrome?
A: Sex Chromosome abnormalities causes turners syndrome. Persons with turners syndrome are…
Q: Explain dimorphism, how it arises, and the problemsit may cause.
A: The condition or property of being dimorphic or dimorphous: like. a: the existence of 2 distinct…
Q: Explain the Wilson’s disease ?
A: To explain: To explain Wilson’s disease and its causes
Q: What is the labeled part of these figures?
A: Answer: SHOOT and ROOT system are the two parts of a plant where shoot includes the upper portion…
Q: Explain down's syndrome?
A: The process of gamete formation involves meiotic division that results in cutting down the…
Q: Describe two spontaneous lesions that can lead tomutations.
A: Mutation can be defined as the phenomenon in which there is a change of the sequence of the genome…
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 is syndrome ? Name three syndromes
A: Disease is defined as any deviation from the normal physiologic function or structure of organism.…
Q: Give a brief explanation of Gauchers disease.What is the inheritance pattern of this disease?
A: Gaucher's disease is inherited genetic condition which occur due to deficiency of enzyme…
Q: Differentiate hypernatremia and hyponatremia. Give 5 causes of each disorder.
A: To comprehend what renal failure is, it is necessary to first understand how the kidneys work and…
Q: What category of genetic disorders does albinism disord
A: Answer Albinism is a single gene defect and it is a type genetical disorder.
Q: What is anomic aphasia?
A: The anomia is generally a language disorder - inability to express or communicate. It will slowly…
Q: Give details of the precise cytogenetic or molecular abnormality of Huntington's Disease.
A: DNA(deoxyribonucleic acid) is defined as the double helix biological molecule where it play a major…
Q: Explain the term sporulation.
A: Reproduction is the process by which the organisms propagate their species by the union of the male…
Q: Explain about dominant negative mutation ?
A: Mutation is any change in the DNA or RNA sequence which may or may not alter the normal functioning…
Q: Can Turner syndrome be cured?
A: The genetic condition characterized by the absence of an X chromosome in the females. The ploidy of…
Q: Besides CFTR, what othe gene is associated with cystic fibrosis?
A: Introduction Cystic fibrosis:- It is an inherited disorder that causes severe damage to the…
Q: What is the cause of Down syndrome?
A: A mutation denotes the manipulation of sequence of the genetic material of a living organism that is…
Q: What is the common cause of the syndromes mentioned below? only pick one and why. a. Williams…
A: A syndrome is defined as a group of symptoms that can appear together. The syndrome is characterized…
Q: What is the most common mitochondrial disease?
A: Mitochondria are cell organelles within eukaryotic cells, which produce adenosine triphosphate…
Q: What are the risk factors for adult NHL?
A: Adult NHL is adult non hodgkins lymphoma is a type of a malignant cancer that starts in the lymph…
Q: What causes short stature in Turner syndrome?
A: Answer: Introduction: Turner syndrome (TS) is commonly found chromosomal disorders. It appears…
Q: What are similarities between Jacob Syndrome and Patau Syndrome?
A: Jacob Syndrome is a chromosomal aberration caused by the non-disjunction of the Y chromosome. They…
Q: What are turner's syndrome?
A: There are various genetic disorders that develop due to anomalies in sex chromosomes. Sometimes the…
Q: Difference between klinefilter syndrome and turner's syndrome?
A: Any gain or loss in the number of chromosomes number, or any change in the structure of the…
Q: Given the information regarding sickle cell anemia, if two carriers were to have children, what…
A: Sickle-cell disease is a condition of the blood wherein the structure of the hemoglobin within the…
Q: effects of the sickle cell disease(inheriting two copi
A: Sickle cell disease is a type of inherited disease. It is caused by a defective gene. When a baby…
Q: Considering the genetics of Lesch–Nyhan syndrome, explain how a female could inherit the disease…
A: Lesch-Nyhan syndrome is a genetic disorder that was categorized by neurological and behavioral…
Q: Explain about Cri du Chat Syndrome in Humans ?
A: The disease is caused when there is a deviation from the normal occurs. Diseases can be communicable…
Q: Explain the “great plate count anomaly.”
A: Microbiological culture is a method of multiplying microorganisms in lab conditions on growth media.…
Q: Indicate how D-value and z-value differ.
A: Introduction A microbe, or microorganism, is a microscopic organism. It may occur as a single-celled…
Q: Define these pairs of terms, and distinguish between them. Patau syndrome/Edwards syndrome
A: Some chromosomal disorders are caused due to change in the number of chromosomes in the offspring.…
Q: What is sickle-cell trait ?
A: Sickle cell disease (SCD) is a genetic disorder caused by mutation in the gene coding for beta…
Q: Can you explain color blindness and hemophilia?
A: Color blindness and hemophilia are X-linked inherited disorders. X-linked inheritance means the…
Explain about the Prader–Willi syndrome ?
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