Accepted at 3:22 p.m. Oct, 31, 2023 by Joe
Author: mero_hero
Related Note: 1521168066019
Rationale for change

The most common genetic cause is cystathionine synthase deficiency. BnB mentions MTHFR in the less common causes.

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Lecture Notes
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Pathoma
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Sketchy

Watch Homocystinuria
Sketchy 2
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Picmonic
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Pixorize

Review Homocysteine Metabolism
Physeo
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Bootcamp
Watch associated Bootcamp video - Homocystinuria: Pathophysiology

Watch associated Bootcamp video - Thrombophilias

Watch associated Bootcamp video - Cystinuria and Organic Acidemias: Cystinuria
OME

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#AK_Step1_v12::#SketchyBiochem::01_Metabolism::02_Amino_Acids_&_Proteins::10_Homocystinuria #AK_Step1_v12::^Other::^EXPN::Boards&Beyond #AK_Step1_v12::^Other::^HighYield::2-RelativelyHighYield #AK_Step1_v12::#B&B::03_Biochem::03_Amino_Acids::03_Other_Amino_Acids #AK_Step1_v12::#FirstAid::01_Biochemistry::05_Nutrition::11_Vitamin_B9 #AK_Step1_v12::#Bootcamp::Biochemistry::10_Protein_Metabolism::10_Cystinuria_and_Organic_Acidemias:_Cystinuria #AK_Step1_v12::#UWorld::COMLEX::24615 #AK_Step1_v12::^Other::^EXPN::BGadd #AK_Step1_v12::#OME::PreClinical::Biochemistry::Biochemistry_1:_DNA_to_Protein::Amino_Acids_Form_Proteins #AK_Step1_v12::#Bootcamp::Biochemistry::06_One_Carbon_Metabolism::07_Homocystinuria:_Pathophysiology #AK_Step1_v12::^Systems::Biochem::BGadds #AK_Step1_v12::#Physeo::05_Biochem::05_Metabolism::17_Homocysteine #AK_Step1_v12::#Bootcamp::Hematology_and_Oncology::07_Coagulation_and_Fibrinolysis::05_Thrombophilias #AK_Original_Decks::Step_1::Zanki_Step_Decks::Zanki_Biochemistry::Vitamins #AK_Step1_v12::#UWorld::Step::788 !AK_UpdateTags::Step1decks::Zanki-Step-Decks::Zanki-Biochemistry::Vitamins #AK_Step1_v12::#FirstAid::01_Biochemistry::05_Nutrition::11_Vitamin_B9::Deficiency #AK_Step1_v12::#B&B::03_Biochem::04_Vitamins::02_Folate_&_Vitamin_B12 !AK_UpdateTags::AnKing_Image::Aiman #AK_Step1_v12::#Pixorize::01_Biochemistry::02_Biochemical_Pathways::17_Homocysteine_Metabolism #AK_Step1_v12::^Other::^EXPN::Uworld #AK_Step1_v12::#AMBOSS::emaxeO