Diabetic ketoacidosis US Medical PG Flashcards - Medical Study Cards
Master Diabetic ketoacidosis with OnCourse flashcards. These spaced repetition flashcards are designed for medical students preparing for NEET PG, USMLE Step 1, USMLE Step 2, MBBS exams, and other medical licensing examinations.
Diabetic ketoacidosis Flashcard Deck - 10 Cards
Flashcard 1: What type of acidosis will a patient with diabetic ketoacidosis experience?_____
Answer: high anion gap metabolic acidosis
Flashcard 2: In the treatment of Diabetic Ketoacidosis and Hyperosmolar Hyperglycemia State, aggressive _____tonic saline fluids are indicated
Answer: iso
Flashcard 3: What is the cause of metabolic acidosis in a patient with diabetes mellitus?_____
Answer: Increased production of ketoacids
Flashcard 4: Does hyperosmolar hyperglycemia non-ketotic syndrome present with acidosis? Why? _____
Answer: No, ketone production is inhibited by presence of insulin
Flashcard 5: One of the most feared complications of type 2 diabetes is _____
Answer: hyperosmolar hyperglycemia non-ketotic syndrome
Flashcard 6: Kallmann syndrome
Answer: defective migration of GnRH cells
Extra: anosmia, lack of secondary sex characteristicsdecreased: GnRH, FSH, LH, testosterone, sperm count
Flashcard 7: Hormone profile in Hypogonadotropic Hypogonadism (LH/FSH and Sex Steroids)
Answer: Decreased LH/FSH and decreased Testosterone/Estrogen
Extra: Hypogonadotropic hypogonadism (secondary hypogonadism) is characterized by low gonadotropins (LH, FSH) which leads to low sex steroid production.
Contrast with Hypergonadotropic hypogonadism (primary): High LH/FSH, low sex steroids.
Flashcard 8: Hormonal profile in primary hypogonadism:
Answer: Increased LH, Decreased Testosterone
Extra: In primary hypogonadism (hypergonadotropic hypogonadism), the problem is at the level of the testes. Loss of negative feedback from testosterone leads to a compensatory rise in LH (and FSH).
Flashcard 9: What is the basic defect in Androgen Insensitivity Syndrome?
Answer: Defect in androgen receptor
Extra: • Genotype: 46, XY (Normal male)
• Phenotype: Female external genitalia, rudimentary/blind-pouch vagina, absent uterus/tubes (due to MIF).
• Gonads: Internal testes (often in labia/inguinal canal).
• Labs: Increased Testosterone, LH, and Estrogen.
• Clinical: Scant sexual hair (distinguishes from Mullerian agenesis).
Flashcard 10: What is the fundamental defect in 5α-reductase deficiency?
Answer: Inability to convert testosterone to DHT (Dihydrotestosterone)
Extra: - Presentation: Male internal genitalia, ambiguous external genitalia until puberty (when increased testosterone leads to virilization).
- Lab findings: Normal testosterone and estrogen; LH normal or slightly increased.
- Inheritance: Autosomal Recessive (AR).
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