Canavan disease - Study guides, Class notes & Summaries

HOSA Pathophysiology exam guide version 2023 with all updates Angelman syndrome - - Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease - - autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease - - protein gluten is not properly broken down cystic fibros...

uWise question bank with complete solutions what are the signs of pulmonary embolus? - Answer- -tachycardia, tachypnea, hypoxia, chest pains, signs of DVT what are the signs of mitral stenosis? - Answer- -diastolic murmur and signs of heart failure which respiratory volumes are increased in pregnancy? - Answer- -inspiratory capacity, tidal volume and minute ventilation which respiratory volumes are decrease in pregnancy? - Answer- -expiratory reserve capacity, functional reserve capacity...

Angelman syndrome - CORRECT ANSWER Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease - CORRECT ANSWER autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease - CORRECT ANSWER protein gluten is not properly broken down cystic fibrosis - CORRECT ANSWER Hered...

Angelman syndrome Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease protein gluten is not properly broken down cystic fibrosis Hereditary condition that causes the exocrine gland...

Angelman syndrome - CORRECT ANSWER Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease - CORRECT ANSWER autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease - CORRECT ANSWER protein gluten is not properly broken down cystic fibrosis - CORRECT ANSWER Hered...

HOSA Pathophysiology ANSWERED CORRECTLY 2023//2024 Angelman syndrome - ANSWER Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease - ANSWER autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease - ANSWER protein gluten is not properly broken down cystic ...

Angelman syndrome - CORRECT ANSWER Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease - CORRECT ANSWER autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease - CORRECT ANSWER protein gluten is not properly broken down cystic fibrosis - CORRECT ANSWER Heredit...

HOSA Pathophysiology Exams Questions and Answers (2023) (Verified Answers) Angelman syndrome - CORRECT ANSWER Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease - CORRECT ANSWER autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease - CORRECT A...

Angelman syndrome - ANSWER Deletion of normally active maternal allele. Mental retardation, seizures, ataxia, inappropriate laughter ("happy puppet") Canavan disease - ANSWER autosomal recessive, chromosome 17 enzyme aspartoacylase hypotonia, poor head control, GE reflux of poor weight gain, demyelination, progressive leukodstrophy, and death in 1st decade coeliac disease - ANSWER protein gluten is not properly broken down cystic fibrosis - ANSWER Hereditary condition that causes the ex...

Stat Pearls Practice Exam Test Questions with Answers A male infant is born with 46 XY karyotype, male internal genitalia, and female external genitalia. Which of the following enzymes is likely to be deficient? Top of Form 1.21-hydroxylase2.5-alpha reductase3.1-alpha-hydroxylase4.Cystathionine synthase - ️️ -b A 17-year-old girl presents to the gynecology department with complaints of amenorrhea. On evaluation, it was found that the girl did not have ovaries, but she had a pair of ...