How can Cri-Du-Chat syndrome be diagnose with karyotyping?

Q: What is the cause of Wolf-Hirschhorn and make sure to explain specifically why the karyotype of your…

A: Wolf-Hirschhorn syndrome (WHS) is a genetic disorder that affects many parts of the body. The major…

Q: Define the common type of gene interaction or Epistxis.

A: Epistasis is a phenomenon in which there is an interaction between genes which influence a…

Q: list two things that the process of karyotyping is used for.

A: Karyotyping is a process used to determine the chromosomal complement of any individual, chromosome…

Q: Do we know what genes cause Down syndrome?

A: In simple words, Gene can be defined as the basic physical and functional unit of heredity. Genes…

Q: What is the basis for spectrum karyotyping?

A: Answer: Introduction:  A karyotype is the method of taking picture of chromosomes and to study its…

Q: Is Miller Fisher syndrome hereditary?

A: Miller Fischer syndrome is a rare acquired nerve disorder that is characterized by abnormal muscle…

Q: What is pseudoagouti (highly methylated) phenotype ?

A: Phenotype generally refers to the observable characteristics of an organism. It is generally…

Q: what is the phenotype of the attached images?

A: Genes are the functional unit of heredity. It carries information from one generation to another.…

Q: What do the 3r's refers to?

A: Natural resources of Earth include water, minerals, soil, air, plants, and wildlife, protection and…

Q: What are holandric genes?

A: Holandric genes are genes that are found on the Y chromosome that are not homologous to any other…

Q: Define what is the Karyotype ?

A: The process in which the chromosomes of an organism are paired and ordered is known as Karyotyping.…

Q: What is a Pericentric inversion?

A: The chromosomes are the thread like structure that contains hereditary information in the form of…

Q: A student has difficulty reading the blackboard while sitting in the last row. What could be the…

A: Eye disorders occur due to changes in the length or shape of the lens, which leads to the formation…

Q: What are the possible genotypes of the PTC locus?

A: * genotype means collection of genes that  refers to two alleles of a particular gene and genotype…

Q: What is the genetic basis of the symptoms of Down syndrome?

A: Ans: In humans various diseases or disorders are caused by chromosomal aberrations or mutation in…

Q: An example of a single gene disorder is O a. Cri-du-chat Syndrome O b. Phenylketournia Patou

A: Cr-du-chat Syndrome : It is a rare genetic disorder which is caused by a missing section on a…

Q: what are treatments for polycystic overy syndrome?

A: Polycystic ovary syndrome is the condition of ovary in which the follicles are solidified to form…

Q: What is Locus heterogeneity?

A: Inheritance of genetic diseases follows a simple Mendelian pattern of inheritance. Its study is…

Q: What is polygenic inheritance? Discuss the issues that make polygenicinheritance difficult to study.

A: A polygene is a member of non epistatic genes group.It interacts to influence a phenotypic…

Q: What is an orthologous gene and How do you get orthologous genes?

A: The homologous gene is a gene inherited by a common ancestor in two different species. It can be…

Q: What is the chromosome abnormality in cri du chat syndrome?

A: Cri-du-chat syndrome, commonly known as 5p- (5p minus) syndrome. Infants with this syndrome…

Q: What is spectral karyotype ?

A: Introduction:- Karyotyping is a test that looks at the chromosomes of a group of cells. This test…

Q: What is genotyping?

A:

Q: physical appearances of individuals affected by the abnormality structure of deletion, inversion,…

A: The phenotypes of individuals are effected by numerous factors. As much as it depends on factors…

Q: What is anomic aphasia?

A: The anomia is generally a language disorder - inability to express or communicate. It will slowly…

Q: How are karyotypes used?

A: Karyotype is the collection of chromosomes which is examined for certain purposes. Chromosomes…

Q: How are genetic variants identified?

A:

Q: How to diagnose aneuploidy?

A: The chromosomes are thread-like structure located in the nuclei of both plant and animal cells. They…

Q: Distinguish among Klinefelter, Down, and Turner syndromes. Which syndromes are found in both sexes?

A: Introduction A genetic condition is an illness caused in part or entirely by a deviation from the…

Q: What are 3 disorders due to Nondisjunction?

A: Disease:   When an organism’s body system does not work properly or any organ affects by viruses,…

Q: what are the steps for diagnosing Cri-Du-Chat syndrome using Karyotyping?

A: The analysis of cri du chat disorder is affirmed by an through clinical assessment, Identification…

Q: What causes short stature in Turner syndrome?

A: Answer: Introduction: Turner syndrome (TS) is commonly found chromosomal disorders. It appears…

Q: Compare and contrast the molecular and phenotypic features of Prader-Willi and Angelman syndromes.

A: Prader villi and angle man syndrome are  imprinting disorders. Both are related to  abnormalities in…

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: Can a male be a carrier of red-green color blindness?  Provide explanation and Punnet square if…

A: Color blindness is defined as the inability of the person to distinguish between colors, especially…

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: What types of chromosomal disorders are easily seen with a karyotype?

A: KARYOTYPE:- It is the complete set of chromosomes of an individual used to check for any…

Q: How do orthologous genes arise?

A:

Q: Can a human male be a carrier of red-green color blindness?

A: The most prevalent types of color blindness are genetic, meaning they are handed down from one…

Q: Is this karyotype male or female? What kind of error (if any) Name of syndrome

A: In karyotype, a picture of the person's chromosomes is taken in order to determine the chromosome…

Q: How do I construct these punnets squares?

A: Punnet square The Punnett square was first time designed by Reginald C. Punnett. It is use to…

Q: Compare and contrast the molecular mechanisms leading to FX syndrome and to FSHMD.

A: Introduction :- A gene originally known as FMR1 gene by scientists and responsible for FXS is…

Mitochondrial Mutations

A mitochondrion is a cellular organelle that serves as the site for cellular respiration and energy production (ATP or Adenosine Triphosphate). It is a double-membrane-bound organelle and is only present in eukaryotic cells.