South University, Savannah - NSG 6435 Week 9 Quiz/Rated A

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Question 1 1 / 1 point A client presents to clinic for the 1st time. The provider discovers that the client was diagnosed w/ Prader-Willi Syndrome. What symptoms does the provider expect to find dur... ing this encounter? Hyperphagia, obesity & strabismus Lethargy, stridor, & irritability Low-set ears, short stature & webbed neck Flat nasal bridge, epicanthal folds, & heart murmur Question 2 0 / 1 point A client w/ Prader-Willi syndrome, well-known to the clinic, presents today for an annual physical. This client is at higher risk & 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 & dental crowding, prominent ears, strabismus, macroorchidism, short stature, cognitive impairments & stereopathies. What would be the most likely diagnosis? Fragile X Prader-Willi Angelman Beckwith-Weidemann Question 4 1 / 1 point If a client is ( + ) for any of the following categorical clinical findings & developmental deficiencies: Failure to thrive, Central obesity, Enamel hypoplasia, Scoliosis, Motor delays, Mild intellectual disability & Compulsive hyperphagia; what would be the most likely diagnosis? Fragile X Prader-Willi Angelman Beckwith-Weidemann Question 5 0 / 1 point If a client is ( + ) for any of the following categorical clinical findings & developmental deficiencies: Seizures, Global developmental delays, abnormal gait, arms held high/flexed elbows, hypOtonic trunk w/ hypERtonic limbs (commando crawl), feeding/growth problems, aquired microcephaly, speech delay, spontaneous (persistent) social smile/fits of laughter & L♥VES water. What would be the most likely diagnosis? Fragile X Prader-Willi Angelman Beckwith-Weidemann Question 6 0 / 1 point If a client is ( + ) for any of the following categorical clinical findings & 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 w/ maxillary underdevelopment & 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 ( + ) for any of the following categorical clinical findings & developmental deficiencies: tall, long limbs, aortic root dilatation, mitral valve prolapse/regurgitation, ectopialentis, myopia, retinal detachment, exotropia/strabismus, spontaneous pneumothorax, connective tissue problems, pectus deformities, joint hyperextensibility. What would be the most likely diagnosis? Turner DiGeorge Marfan Huntington Question 8 1 / 1 point What is true about diploid cells? (SATA) Each contains 23 paired chromosomes. Each one contains 23 chromosomes. Replication produces two identical cells. They replicate via the process of mitosis. Question 9 1 / 1 point Cystic fibrosis is a genetic disorder that affects the cells that produce mucus, sweat & digestive juices. It is considered a recessive disease caused by a gene mutation on both alleles inherited from the parents. Which GenDisorder is this? Chromosome Mitochondrial Monogenetic Multifactorial Question 10 1 / 1 point Which diagnostic test is most appropriate when a provider wishes to identify & evaluate the size, shape & number of chromosomes of a client? Chromosomal microarray Fluorescence in-situ hybridization Karyotype Molecular testing Prader–Willi Syndrome: PCSK1 deficiency, obesity, hyperphagia, hypothalamus [Show More]

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