X-Git-Url: http://unremediatedgender.space/source?p=Ultimately_Untrue_Thought.git;a=blobdiff_plain;f=notes%2Ftrans-kids-on-the-margin-notes.md;fp=notes%2Ftrans-kids-on-the-margin-notes.md;h=2fca30c97e0dbd85422771247f5893213d4e3fd4;hp=d99ee5fc9e2f5186c4be9ec91bb643bae310c099;hb=f05a6cc7459189162e841f5b5dd090ad69a5bdf4;hpb=bb9203e102e4456df500e11d1766aff6badac098

diff --git a/notes/trans-kids-on-the-margin-notes.md b/notes/trans-kids-on-the-margin-notes.md
index d99ee5f..2fca30c 100644
--- a/notes/trans-kids-on-the-margin-notes.md
+++ b/notes/trans-kids-on-the-margin-notes.md
@@ -295,7 +295,7 @@ SRY was discovered when discovered in an XX male
 
 CAH occurs is autosomal and occurs in both males and females, but the reason we only talk about CAH girls is that the effects on boys are less noticeable
 
-> CYP21 is on chromosome 6 and encodes an enzyme normally present in the adrenal gland called 21-hydroxylase (21-OH). Individuals with CAH due to 21-OH defi ciency are unable to produce enough cortisol to suppress the release of adrenocorticotropic hormone (ACTH). This results in an accumulation of products that normally become cortisol, which in turn results in increased production of androgen from the adrenal gland. This excess androgen has many of the same effects as testosterone produced by the testes in males
+> CYP21 is on chromosome 6 and encodes an enzyme normally present in the adrenal gland called 21-hydroxylase (21-OH). Individuals with CAH due to 21-OH deficiency are unable to produce enough cortisol to suppress the release of adrenocorticotropic hormone (ACTH). This results in an accumulation of products that normally become cortisol, which in turn results in increased production of androgen from the adrenal gland. This excess androgen has many of the same effects as testosterone produced by the testes in males
 
 There's a gradation in CAH—you can have a little 21-OH, or none at all