Angelman syndrome - Study guides, Class notes & Summaries
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HOSA Pathophysiology exam guide version 2023 with all updates
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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...
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MCMB Test Questions with Correct Answers
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MCMB Test Questions with Correct Answers 
 
Angelman Syndrome - Answer-15q maternal deletion (UBE3A) 
 
Carrier mother may give to either gender kid 
Carrier father will not give to either kid (daughter may carry) 
 
Prader Willi - Answer-15q paternal deletion (SNORD) 
 
NIPS - Answer-after 7 wks 
common autosomal and sex aneuploidies 
 
CVS - Answer-10-13 wks 
Same as amniocentesis results 
 
Amniocentesis - Answer-16-20 wks 
Alpha-fetoprotein 
chromosome and genome analysis 
 
Preimplantation ...
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HOSA Pathophysiology Exams Questions and Answers (2023) (Verified Answers)
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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...
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PEDS FINAL EXAM Practice Q's with 100% correct answers
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-----------WEEK 9------ 
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? 
>>Hyperphagia, obesity, and strabismus 
 
Lethargy and stridor and irritability 
 
Low-set ears, short stature, webbed neck 
 
Flat nasal bridge, epicanthal folds and heart murmur 
 
 
 
Prader-Willi Syndrome 
1) Caused by a lack of genetic material in the 15 pair of c...
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HOSA Pathophysiology Exams 2023 Questions and Answers (2023) (Verified Answers)
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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...
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MTM Exam 4 Diseases Latest Update with Verified Solutions
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MTM Exam 4 Diseases Latest Update with Verified Solutions 
DMD -loss of function, recessive, haplosufficiency -symptoms present < 5 yoa -progressive symmetrical muscular weakness -wheelchair dependent by 12-13 yoa -life expectancy = teens - 30s -do not reproduce -calf pseudohypertrophy -elevated serum creatine kinase -unable to perform neck flexion -complete absence of dystrophin -mutations: deletions, frameshift, nonsense -exon length is NOT a multiple of 3 -frameshifts -> null mutations ...
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CBSE High Yielding/Mnemonics/Cases with Detailed Answers for Exam Review
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Cerebellar ataxia, telangiectasias, and increased risk of sinopulmonary infections = triad of _________. 
-This is due to a defect in the ________gene responsible for ____________. 
-immune deficiency manifests as _______ - ***ataxia telangiectasia 
ATM gene responsible for DNA break repair 
IgA deficiency 
Pt presents with unsteady gait, spider like capillary angiomas on the skin, and recent pulmonary 
infections...Dx= - ***Ataxia Telangiectasia 
Pt presents with Thrombocytopenia, Eczema, an...
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NR 507 ADVANCED PATHOPHYSIOLOGY MIDTERM EXAM QUESTIONS AND COMPLETE WELL EXPLAINED ANSWERS WITH RATIONALES 100% CORRECT AND VERIFIED BY EXPERTS GRADED A+ LATEST UPDATE 2024 (SUCCESS GUARANTEED]ALL YOU NEED TO PASS YOUR EXAMS
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NR 507 ADVANCED PATHOPHYSIOLOGY MIDTERM EXAM QUESTIONS AND COMPLETE WELL EXPLAINED ANSWERS WITH RATIONALES 100% CORRECT AND VERIFIED BY EXPERTS GRADED A+ LATEST UPDATE 2024 (SUCCESS GUARANTEED]ALL YOU NEED TO PASS YOUR EXAMS 
 
What is epigenetics?	The study of heritable changes in gene expression or phenotype casued by mechanisms *other* than changes in DNA sequences. 
DNA methylation	The attachment of a methyl group to a cytosine base is followed by a guanine base...causes a gene to become t...
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NR507 2023 Midterm Exam Questions with Correct Answers
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NR507 2023 Midterm Exam Questions with Correct Answers 
Epigenetics - ANSWER heritable alterations that are not due to changes in DNA sequence 
 
epigenetic modifications, or "tags," such as DNA methylation and histone modification - ANSWER alter DNA accessibility and chromatin structure, thereby regulating patterns of gene expression. 
 
histone modifications - ANSWER A histone modification is a covalent post-translational modification (PTM) to histone proteins whi...
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NR 507 Week 4 Midterm (Actual Exam)
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1.	Question: A 10 year old male is stung by a bee while playing in the yard. He experiences a severe allergic reaction and has to go to the ER. The nurse providing care realizes this reaction is the result of: 
2.	Question: Chronic bronchitis is characterized by: 
3.	Question: A 6 year old female is ... with a bacterial infection of the respiratory system. Which of the following will most likely try to fight the antigen? 
4.	Question: A 52 year old male is ... with urinary tract obstruction. Whi...
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