NSG 6435Week 9 Quiz (Graded A+) LATEST UPDATE

NSG 6435Week 9 Quiz Week 9 Quiz Question 1 0 / 1 point A client presents to clinic for the first time. The provider discovers that the client was diagnosed with Prader-Willi Syndrome. What symptoms does the provider expect to find during this encounter? Hyperphasia, obesity, and strabismus Lethargy, stridor, and irritability Low-set ears, short stature, and webbed neck Flat nasal bridge, epicanthal folds, and heart murmur Question 2 0 / 1 point A client with Prader-Willi syndrome, well-known to the clinic, presents today for an annual physical. This client is at higher risk and should be screened for what medical condition? Depression Pyloric Stenosis Celiac disease Type 2 diabetes mellitus Question 3 0 / 1 point A new client presents to the clinic to establish care. On exam, the provider notes the following: a long narrow face, high-arched palate and dental crowding, prominent ears, strabismus, macroorchidism, short stature, cognitive impairments and stereopathies. What would be the most likely diagnosis? Fragile X Prader-Willi Angelman Beckwith-Weidemann Question 4 1 / 1 point If a client is positive for any of the following categorical clinical findings and developmental deficiencies: Failure to thrive, Central obesity, Enamel hypoplasia, Scoliosis, Motor delays, Mild intellectual disability and Compulsive hyperphagia; what would be the most likely diagnosis? Fragile X Prader-Willi Angelman Beckwith-Weidemann View Feedback Question 5 0 / 1 point If a client is positive for any of the following categorical clinical findings and developmental deficiencies: Seizures, Global developmental delays, Abnormal gait, arms held high/flexed elbows, Hypotonic trunk with hypertonic limbs (commando crawl), Feeding/growth problems, Acquired microcephaly, Speech delay, Spontaneous (persistent) social smile/fits of laughter, and Loves water. What would be the most likely diagnosis? Fragile X Prader-Willi Angelman Beckwith-Weidemann Question 6 0 / 1 point If a client is positive for any of the following categorical clinical findings and developmental deficiencies: Omphalocele or umbilical hernia, macroglossia, facial features: Nevus flammeus, helical pits, prominent eyes, anterior ear lobe creases, Large placenta/long umbilical cord, Hypoglycemia, Cardiomegaly, Dental malocclusion with maxillary underdevelopment, and Articulation issues. What would be the most likely diagnosis? Fragile X Prader-Willi Angelman Beckwith-Weidemann Question 7 1 / 1 point If a client is positive for any of the following categorical clinical findings and developmental deficiencies: tall, long limbs, aortic root dilatation, mitral valve prolapse/regurgitation, ectopia lentis, myopia, retinal detachment, exotropia/strabismus, spontaneous pneumothorax, connective tissue problems, pectus deformities, joint hyperextensibility. What would be the most likely diagnosis?What would be the most likely diagnosis? Turner DiGeorge Marfan Huntington View Feedback Question 8 0 / 1 point What is true about diploid cells? (select all that apply) Each contains 23 paired chromosomes. Each one contains 23 chromosomes. Replication produces two identical cells. They replicate via the process of mitosis. View Feedback Question 9 0 / 1 point Cystic fibrosis is a genetic disorder that affects the cells that produce mucus, sweat, and digestive juices. It is considered a recessive disease caused by a gene mutation on both alleles inherited from the parents. Which type of genetic disorder is this? Chromosome Mitochondrial Monogenetic Multifactorial Question 10 1 / 1 point Which diagnostic test is most appropriate when a provider wishes to identify and evaluate the size, shape, and number of chromosomes of a client? Chromosomal microarray Fluorescence in-situ hybridization Karyotype Molecular testing Hide Feedback Karyotype testing is used to identify and evaluate the size, shape, and number of chromosomes