need help with your account or subscription? click here to email us (or see the contact page)
join telegramNEW! discord
jump to exam page:
search for anything ⋅ score predictor (โ€œpredict me!โ€)

NBME 20 Answers

nbme20/Block 2/Question#25 (reveal difficulty score)
A 14-year-old girl is brought to the ...
Mitochondrial tRNALeu ๐Ÿ” / ๐Ÿ“บ / ๐ŸŒณ / ๐Ÿ“–
tags: MELAS Biochem

 Login (or register) to see more


 +19  upvote downvote
submitted by โˆ—sympathetikey(1600)
get full access to all contentpick a username

Mutations in MT-TL1 (Mitochondrially encoded tRNA leucine 1)

A common mutation is A3243G. Can result in multiple mitochondrial deficiencies and associated disorders. It is associated with:

  • Mitochondrial encephalomyopathy
  • Lactic acidosis
  • Stroke-like episodes (MELAS)

MELAS is a rare mitochondrial disorder known to affect many parts of the body, especially the nervous system and the brain. Symptoms of MELAS include:

  • Recurrent severe headaches
  • Muscle weakness (myopathy)
  • Hearing loss
  • Stroke-like episodes with a loss of consciousness, seizures, and other problems affecting the nervous system.

Source: https://en.wikipedia.org/wiki/MT-TL1

get full access to all contentpick a username
j44n  i just saw that every tissue that was affected had a high 02/aTP requirement and mixed with the lactic acid that meant she wasnt using her electron transport chain so i picked the only answer that had mitochondria in it +6
topgunber  The disease is MELAS. Mitochondrial encoded tRNA leucine 1 is the mutation. Apparently associated with high tone deafness. It is apparent its mitochondrial with maternal transmission, though unfortunately the etiology is utter memorization / process of elimination. Maybe next time the stragy will focus more on mitochondiral diseases and see that this choice is the only mitochondiral answer choice. Mitochondrial Encephalomyopathy Lactic Acidosis Stroke like symptoms."MELAS is a rare mitochondrial disorder known to affect many parts of the body, especially the nervous system and the brain. Symptoms of MELAS include recurrent severe headaches, muscle weakness (myopathy), hearing loss, stroke-like episodes with a loss of consciousness, seizures, and other problems affecting the nervous system.[5]" Source :Wiki +



 +12  upvote downvote
submitted by mrmassador(12)
get full access to all contentpick a username

I think the point of the question is to recognize that this is a mitochondrial disease (mother and maternal grandmother were affected). Produces wide range of effects, but muscle weakness and some neurologic deficits stood out to me. Also this: https://ghr.nlm.nih.gov/gene/MT-TL1#conditions

get full access to all contentpick a username
sympathetikey  Yes, but doesn't that mean maternal transmission? Men can have these diseases too, they just won't pass them on. +32



 +5  upvote downvote
submitted by โˆ—hayayah(1212)
get full access to all contentpick a username

This is a presentation of mitochondrial myopathy. They often present with myopathy, lactic acidosis, and CNS disease. 2ยฐ to failure in oxidative phosphorylation. Muscle biopsy often shows โ€œragged red fibersโ€.

There is variable expression in a population or even within a family due to heteroplasmy in mitochondrial inheritance.

get full access to all contentpick a username



 +1  upvote downvote
submitted by thomas(3)
get full access to all contentpick a username

It's a mitochondrial disease. - present in successive generations, always with maternal transmission - damage to high-energy tissues - CSF lactic acidosis (due to increased anaerobic metabolism due to impaired oxidative phosphorylation)

get full access to all contentpick a username



 +1  upvote downvote
submitted by โˆ—topgunber(67)
get full access to all contentpick a username

The disease is MELAS. Mitochondrial encoded tRNA leucine 1 is the mutation. Apparently associated with high tone deafness. It is apparent its mitochondrial with maternal transmission, though unfortunately the etiology is utter memorization / process of elimination. Maybe next time the stragy will focus more on mitochondiral diseases and see that this choice is the only mitochondiral answer choice.

  • Mitochondrial Encephalomyopathy Lactic Acidosis Stroke like symptoms."MELAS is a rare mitochondrial disorder known to affect many parts of the body, especially the nervous system and the brain. Symptoms of MELAS include recurrent severe headaches, muscle weakness (myopathy), hearing loss, stroke-like episodes with a loss of consciousness, seizures, and other problems affecting the nervous system.[5]" Source :Wiki
get full access to all contentpick a username



Must-See Comments from nbme20

amorah on Cytomegalovirus infection
masonkingcobra on Contact with parakeets
hayayah on Capillary hydrostatic: increased; ...
hayayah on X chromosome-linked isoenzymes
medbitch94 on Mannose 6-phosphate
hello on Capillary hydrostatic: increased; ...
hayayah on Osteoblasts
imgdoc on Hypophosphatemia
hayayah on Missense
celeste on 50%
justgettinby on Omeprazole
andrewk1 on Cold, dry air
yotsubato on Jugular venous pressure of 12 mm Hg
strugglebus on Drug effect

search for anything NEW!