Paediatric - Endocrine and reproductive Flashcards

1
Q

What is the most common cause of thyrotoxicosis?

A

Graves’ Disease

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2
Q

Name a risk factor for developing Hyperthyroidism

A

Family history, High iodine intake, Smoking, Thyroid trauma, Toxic multinodular goitre, Childbirth, Highly active antiretroviral therapy

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3
Q

Name 6 symptoms/signs of hyperthyroidism

A

Symptoms: Weight loss or gain, increased or decreased appetite,Increased or decreased appetite, Irritability, Weakness and fatigue, Diarrhoea, Sweating, Tremor, Heat intolerance, Loss of libido, Oligomenorrhoea or amenorrhoea
Signs: Palmar erythema, Sweaty palms, Fine tremor, Tachycardia, Hair thinning/alopecia, Urticaria, pruritus, Brisk reflexes, Goitre, Proximal myopathy, Gynaecomastia, Lid lag

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4
Q

Which autoantibodies might present in Graves’ disease?

A

Thyroid peroxidase antimicrosomal antibodies, Antithyroglobulin antibodies, TSH-receptor antibodies

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5
Q

Name 2 antithyroid drugs as well as the treatment of choice in relapsed Graves’

A

Carbimazole and Propylthiouracil; radio-Iodine

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6
Q

Name 3 symptoms of Hypothyoidism

A

Tiredness, Weight gain, Constipation, Aches, Feeling cold, Dry skin, Dull or coarse hair, Fluid retention, Mental slowing, Depression, hoarse voice, Irregular or heavy periods, Infertility, Loss of sex drive, Carpal tunnel syndrome

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7
Q

What is the most common cause of hypothyroidism in the UK?

A

Autoimmune Thyroiditis

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8
Q

What is the most common cause of hypothyroidism worldwide?

A

Iodine deficiency

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9
Q

What is the first-line treatment of hypothyroidism?

A

Levothyroxine

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10
Q

Congenital Adrenal Hyperplasia follows what inheritance pattern?

A

Autosomal recessive

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11
Q

Most cases of Congenital Adrenal Hyperplasia are caused by what enzyme deficiency?

A

21-hydroxylase deficiency

others = 11-beta-hydroxylase deficiency

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12
Q

How is deficiency of glucocorticoids and mineralocorticoids treated in classic congenital adrenal hyperplasia?

A

Glucocorticoids: Hydrocortisone
Mineralocorticoids: Fludrocortisone

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13
Q

CAH causes underproduction of what hormones and overproduction of what hormones?

A

cortisol + aldosterone; Androgens

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14
Q

Name the main glucocorticoid hormone

A

Cortisol

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15
Q

Name the main mineralocorticoid hormone

A

Aldosterone

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16
Q

What is 21-hydroxylase responsible for converting?

A

Progesterone into Aldosterone/Cortisol

17
Q

Name a cause of Hyperaldosteronism (Conn’s Syndrome)

A

Adrenal adenoma, Adrenal hyperplasia, Familial hyperaldosteronism, Adrenal carcinoma

18
Q

Name a classic feature of hyperaldosteronism (Conn’s syndrome)

A

Hypertension / Hypokalaemia / Metabolic alkalosis / Sodium normal or slightly raised

19
Q

Name an aldosterone antagonist used in the treatment of Conn’s syndrome

A

Spironolactone / Eplerenone

20
Q

A phaeochromocytoma is a rare tumour that secretes what?

A

Catecholamines (epinephrine (adrenaline), norepinephrine (noradrenaline), and dopamine)

21
Q

Which condition has a classic presentation of Primary Amenhorroea and on examination of the abdomen you can feel two masses in the groin

A

Androgen Insensitivity

22
Q

In most cases the testes will descend by what age?

A

By 3-6 months

23
Q

What surgery is performed on undescended testes after 6 months old?

A

Orchidopexy (surgical correction of undescended testes)

24
Q

A syndrome characterized by delayed or absent puberty and an impaired sense of smell. This disorder is a form of hypogonadotropic hypogonadism

A

Kallman Syndrome

25
Q

long-term administration of what type of drugs may cause adrenal insufficiency?

A

Corticosteroids

26
Q

What are some symptoms of Addison’s crisis?

A
  • Severe vomiting and diarrhoea.
  • Pains in the back and abdomen.
  • Lack of fluid in the body (dehydration).
  • Low blood pressure.
  • Collapse.
27
Q

What is the name for primary adrenal insufficiency?

A

Addison’s disease

28
Q

What stimulates secretion of IGF-1 and where does this take place?

A

GH from anterior pituitary stimulates release of IGF-1 from liver