17q12, explained for kidsdeletion syndrome · static snapshot
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17q12 microdeletion syndrome - Rare Awareness Rare Education Portal

17q12 microdeletion syndrome is a chromosomal condition in which a small part of chromosome 17 is missing (deleted). 1 This small deletion, also known as a microdeletion, occurs at a location on chromosome 17 called 17q12.

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Indexed from **web** on 2026-11-13 (relevance 1.00, tier curated).

Generated 2026-11-13, last changed today. Dedup key newdoc:566. The engine re-checks this insight on every analysis run; if more sources agree, its corroboration and confidence go up and it reappears as “new”.

Evidence (1 quote)

17q12 microdeletion syndrome - Rare Awareness Rare Education Portal curated · published 2025-08-01 · live page
In rare cases, the deletion was inherited from a parent in an autosomal dominant manner (there is a 50% chance that an affected parent will pass it to each of their children).

Supporting documents (1)

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17q12 microdeletion syndrome - Rare Awareness Rare Education Portal web 2025-08-01 today 1.00