100% satisfaction guarantee Immediately available after payment Both online and in PDF No strings attached
logo-home
CBSE Exam Study With Complete Questions And Verified Accurate Answers. $13.49   Add to cart

Exam (elaborations)

CBSE Exam Study With Complete Questions And Verified Accurate Answers.

 28 views  0 purchase
  • Course
  • NBME CBSE
  • Institution
  • NBME CBSE

Alkaptonuria - correct answer Absence of homogentisate oxidase - arthritis - discolored sclerae and other areas (ear cartilage) - Dark urine - spinal disc degeneration and dense calcifications possible What is the cause of "bitter almond" brea...

[Show more]

Preview 3 out of 16  pages

  • June 12, 2024
  • 16
  • 2023/2024
  • Exam (elaborations)
  • Questions & answers
  • NBME CBSE
  • NBME CBSE
avatar-seller
RealGrades
CBSE Exam
Alkaptonuria - correct answer Absence of homogentisate oxidase
- arthritis
- discolored sclerae and other areas (ear cartilage)
- Dark urine
- spinal disc degeneration and dense calcifications possible
What is the cause of "bitter almond" breath? - correct answer Cyanide poisoning
What does cyanide inhibit? - correct answer Cytocrhome oxidase in the ETC
What is the treatment for cyanide poisoning? - correct answer Amyl nitrate (oxidizes hemoglobin to methemoglobin, which strongly binds cyanide)
6 month old child with frequent infections and carpopedal spasm and facial spasm upon tapping - correct answer DiGeorge Syndrome
- hypoparathyroidism and T-cell deficiency
Hypocalcemia is what causes the spasms
CATCH22 pneumonic: Chromosome 22, Abnormal facies, Thymic hypoplasia, Cleft palate, and Hypocalcemia
Young (27 yrs old) man with lots of atherosclerotic plaques and small, raised yellow-brown lesions on extensor surfaces of arms - correct answer Familial hypercholesterolemia (FH) Inherited disorder that causes high serum cholesterol levels
the lesions are xanthomas caused by deposits of the cholesterol
A baby is born with severe abnormalities, including prominent epicanthal folds, up slanting palpebral fissures, and macroglossia. He also has thick skin at the nape of the neck
He vomits greenish material immediately after eating - correct answer Down Syndrome
The vomiting is due to GI disorder which they often have
Boy is born with flat feet, long face, large ears, and an abnormal appearing X-chromosome - correct answer Fragile X syndrome
Expansion of a CGC trinucleotide repeat sequence on the X chromosome
X-linked genetic
The most common cause of mental retardation is - correct answer Fragile X syndrome
A baby begins to get sick after weaning from breast milk, and has a low glucose level which is not lost in urine - correct answer Fructose intolerance
Fructose-1-phosphate levels will be elevated in liver cells
A 12 year old intellectually disabled boy presents with vision difficulties. Exam reveals bilateral dislocated lenses and a tall, thin body habitus. Labs show increased levels of serum methionine and serum homocysteine - correct answer Homocysteinuria caused by cystathionine synthase Also at risk for CV disease and osteoporosis
HOMOCY
Homocyteine in urine, osteoporosis, marfoid habitus, ocular changes, kYphosis
Can also be intellectually disabled
1 year old presents with abnormalities. PE reveals developmental delay, coarse facial features, skeletal abnormalities, umbilical hernia, corneal clouding. Baby's liver and spleen are enlarged, and the joints are
stiff - correct answer Hurler Syndrome
One of the mucopolysaccharidoses diseases
Caused by alpha L-iduronidase defect (can't break down dermatin sulfate and heparan sulfate - accumulates in tissues)
Hunter's Syndrome vs Hurler's Syndrome - correct answer Hunters = mild Hurler's + aggressive behavior, no corneal clouding
2 year old with mental retardation and restricted joint movement. PE reveals coarse facial features and clouded corneas. Blood tests reveal elevated lysosomal enzymes in the serum. Parents are first cousins - correct answer I-cell disease
Similar to Hurler syndrome but with findings at birth First cousins just says that there is an increased risk of an autosomal recessive trait being passed Mutation of the golgi apparatus which keeps a marker from being added to proteins destined for lysosomes

The benefits of buying summaries with Stuvia:

Guaranteed quality through customer reviews

Guaranteed quality through customer reviews

Stuvia customers have reviewed more than 700,000 summaries. This how you know that you are buying the best documents.

Quick and easy check-out

Quick and easy check-out

You can quickly pay through credit card or Stuvia-credit for the summaries. There is no membership needed.

Focus on what matters

Focus on what matters

Your fellow students write the study notes themselves, which is why the documents are always reliable and up-to-date. This ensures you quickly get to the core!

Frequently asked questions

What do I get when I buy this document?

You get a PDF, available immediately after your purchase. The purchased document is accessible anytime, anywhere and indefinitely through your profile.

Satisfaction guarantee: how does it work?

Our satisfaction guarantee ensures that you always find a study document that suits you well. You fill out a form, and our customer service team takes care of the rest.

Who am I buying these notes from?

Stuvia is a marketplace, so you are not buying this document from us, but from seller RealGrades. Stuvia facilitates payment to the seller.

Will I be stuck with a subscription?

No, you only buy these notes for $13.49. You're not tied to anything after your purchase.

Can Stuvia be trusted?

4.6 stars on Google & Trustpilot (+1000 reviews)

80461 documents were sold in the last 30 days

Founded in 2010, the go-to place to buy study notes for 14 years now

Start selling
$13.49
  • (0)
  Add to cart