Welcome to Anagrammer Crossword Genius! Keep reading below to see if debars is an answer to any crossword puzzle or word game (Scrabble, Words With Friends etc). Scroll down to see all the info we have compiled on debars.
debars
Searching in Crosswords ...
The answer DEBARS has 12 possible clue(s) in existing crosswords.
Searching in Word Games ...
The word DEBARS is VALID in some board games. Check DEBARS in word games in Scrabble, Words With Friends, see scores, anagrams etc.
Searching in Dictionaries ...
Definitions of debars in various dictionaries:
verb - bar temporarily
verb - prevent the occurrence of
verb - prevent from entering
more
Word Research / Anagrams and more ...
Keep reading for additional results and analysis below.
| Possible Crossword Clues |
|---|
| Keeps out |
| Prohibits |
| Excludes or prohibits |
| Excludes |
| Precludes |
| Bans beards |
| Refuses to admit sister's sleeping around? |
| Excludes, legally |
| Possible Dictionary Clues |
|---|
| Third-person singular simple present indicative form of debar. |
| exclude or prohibit (someone) officially from doing something. |
| Exclude or prohibit (someone) officially from doing something. |
| Debars might refer to |
|---|
| De Barsy syndrome is a rare autosomal recessive genetic disorder. Symptoms include cutis laxa (loose hanging skin) as well as other eye, musculoskeletal, and neurological abnormalities. It is usually progressive, manifesting side effects that can include clouded corneas, cataracts, short stature, dystonia, or progeria (premature aging).It was first described in 1967 by De Barsy et al. and, as of 2011, there have been 27 cases reported worldwide. The genes that cause De Barsy syndrome have not been identified yet, although several studies have narrowed down the symptoms' cause. A study by Reversade et al. has shown that a mutation in PYCR1, the genetic sequence that codes for mitochondrial enzymes that break down proline, are prevalent in cases of autosomal recessive cutis laxa (ARCL), a condition very similar to De Barsy syndrome. A study by Leao-Teles et al. has shown that De Barsy syndrome may be related to mutations in ATP6V0A2 gene, known as ATP6V0A2-CDG by the new naming system.Alternative names for De Barsy syndrome include corneal clouding-cutis laxa-mental retardation, cutis laxa-growth deficiency syndrome, De Barsy–Moens–Diercks syndrome, and progeroid syndrome of De Barsy. |