Conditions Observed

Breast cancerDuctal Carcinoma (Breast)
CancerOvary Neoplasm
 Testicular Neoplasm
CardiovascularProthrombin (G20210A Mutation)
Digestive systemConstipation
 Familial Intrahepatic Cholestasis
Drug ReactionsCongenital Heart Defect due to Maternal Periconception – SSRIs
 Reactions with the use of antidepressants (SSRI)
Endocrine systemHyperthyroidism
 Transient Neonatal Diabetes
GeneralLonger Menstrual Cycle Duration
 Menstrual Migraine
Hematologic systemCongenital afibrinogenemia
Hereditary diseasesFragile X Syndrome
HormoneAnti-Müllerian hormone (AMH)
 Dihydrotestosterone (DHT)
 FSH deficiency
 Luteinizing Hormone (LH)
 SHBG levels
 Isolated Follicle Stimulating Hormone Deficiency (FSH)
Immune systemAnti-Beta-2-Glycoprotein Antibody
 Antiphospholipid Antibody Syndrome
 Antithrombin Deficiency
 Defect in Thyroid Hormonogenesis
 Factor V Leiden Mutation
 Mutation of the SERPINE1 Gene (PAI-1)
 Prolactin Promoter Polymorphism
 Protein C Deficiency
 Protein S Deficiency
MethylationMTHFR 1298 mutation (rs1801131)
 MTHFR 677 mutation (rs1801133)
PsychiatricPostpartum depression
Reproductive systemAzoospermia
 Azoospermia não obstrutiva
 Erectile Dysfunction
 Erectile Dysfunction after Radiotherapy for Prostate Cancer
 FSH levels
 Female Infertility
 Gestational diabetes
 In vitro fertilization
 Increased Excitation Levels
 Infertility in Endometriosis
 Intra-Hepatic Pregnancy Cholestasis
 Male infertility
 Male precocious puberty
 Neural Tube Defect
 Ovarian Hyperstimulation Syndrome
 Ovarian Response to Hormonal Stimulation
 Pelvic Organ Prolapse
 Peyronie’s disease
 Polycystic Ovary Syndrome
 Premature Ovarian Insufficiency
 Risk of Recurring Pregnancy Loss
 Sexual Motivation (Female)
 Spontaneous abortions
 Uterine Fibroids
 Uterine Fibromyoma
Skeletal system (bones)Development Defects
SkinHereditary Chronic Mucocutaneous Candidiasis
Vitamins needRiboflavin Deficiency