South University, Savannah - NSG 6435

Question1)A client presents to clinic for the 1^st time. The provider discovers that the client was diagnosed w/ Prader-Willi Syndrome. What symptoms does the provider expect to find during this encounter?

Question 2                                                                                                                                                                               

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?

Question 3

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?

Question 4

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?

Question 5                                                                                                                                                                                                

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?

Question 6

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?