Endocrine Problems in Childhood Flashcards

1
Q

Discuss the identification and management of hypothyroidism in the newborn.

A

a

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2
Q

Name common non-pathological causes of short stature.

A
  • Familial
  • Constitutional
  • SGA/IUGR
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3
Q

Name pathological causes of short stature.

A
  • Undernutrition
  • Chronic illness (JCA, IBD, Coeliac)
  • Iatrogenic (steroids)
  • Psychological and social
  • Hormonal (GHD, hypothyroidism)
  • Syndromes (Turner, P-W)
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4
Q

Define early and delayed puberty for both males and females.

A

Males;

  • Early <9 (rare)
  • Delayed >14 (common, especially CDGP)

Females;

  • Early <8 years
  • Delayed >13 (rare)
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5
Q

Main points in Constitutional delay of growth and development (CDGP).

A
  • Mainly males
  • Family history in father or brother(s) (difficult to obtain)
  • Due to bone age delay
  • Need to exclude organic disease
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6
Q

Name other causes of delayed puberty.

A
  • Gonadal dysgenesis (Turner 45X, Klinefelter 47XXY)
  • Chronic disease (Crohn’s, asthma)
  • Impaired HPG axis (septo-optic dysplasia, craniopharyngioma, Kallman’s syndrome)
  • Peripheral (cryptorchidism, testicular irradiation)
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7
Q

Name the conditions of early sexual development.

A

Breast development;

  • Infantile thelarche
  • Thelarche variant (premature thelarche)
  • True central precocious puberty

Secondary sexual characteristics;

  • exaggerate adrenarche
  • Precocious pseudo puberty

PV bleeding;
- Premature menarche

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8
Q

Main points of central precocious puberty.

A
  • Growth spurt
  • Advanced bone age

Girls;

  • Breast development
  • Usually idiopathic
  • Pituitary imaging

Boys;

  • Testicular enlargement
  • Look for underlying cause (?brain tumour)

Treatment: GnRH agonist

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9
Q

Main points of precious pseudopuberty.

A
  • Gonadotrophin independent (low/prepubertal levels of LH and FSH)
  • Abnormal sex steroid hormone secretion
  • Virilasing or feminasing
  • Clinical picture: secondary sexual characteristics
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10
Q

Describe the management approach to ambiguous genitalia.

A
  • Do not guess the sex of the baby!
  • MDT approach (paed endo, surg, neonatologist, geneticist, psychologist)
  • Examine gonads?/ internal organs
  • Karyotype
  • Exclude congenital adrenal hyperplasia! - risk of adrenal crisis is first 2 weeks of life
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11
Q

Summarise congenital hypothyroidism.

A
  • 1 in 4000 births
  • Causes: athyreosis/hypoplastic/ectopic
  • Dyshormonogenic
  • Newborn screening
  • Start treatment within first 2 weeks
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12
Q

Summarise acquired hypothyroidism.

A
  • Most common cause: autoimmune (Hashimoto’s) thyroiditis
  • Family history of thyroid/ autoimmune disorders

Childhood issues;

  • Lack of height gain
  • Pubertal delay (or precocity)
  • Poor school performance (but works steadily)
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13
Q

Describe the assessment of obesity.

A
  • Weight
  • BMI = kg/m2
  • Height
  • Waist circumference
  • Skin folds
  • History and examination
  • Complications
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14
Q

Names causes of obesity.

A
  • SIMPLE OBESITY
  • Hypothalamic damage

Syndromes;

  • Prader Willi syndrome
  • Laurence-Moon-Biedl syndrome
  • Pseudohypoparathyroidism type 1
  • Down’s syndrome

Drugs;

  • Insulin
  • Steroids
  • Antithyroid drugs
  • Sodium valproate

Endocrine disorders;

  • Hypothyroidism
  • Growth hormone deficiency
  • Glucocorticoid excess
  • Hypothalamic lesion (tumour/trauma/infection)
  • Androgen excess
  • Insulinoma
  • Insulin resistance syndromes
  • Leptin deficiency
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