Module 11 - Endocrine Behaviors Flashcards

1
Q

Physiological growth disturbances

A

Short stature, familial
Constitutional growth delay
SGA/IUGR

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2
Q

epidemiology,

-3- -4- is characterized by decreased growth velocity and delayed skeletal maturation in the absence of other explanations.
Human -3- is produced by the -1-. Secretion is stimulated by -3–releasing hormone and inhibited by -2-. Features of infantile -3- -4- include normal birth weight and slightly reduced length, hypoglycemia (if accompanied by adrenal insufficiency), micropenis (if accompanied by gonadotropin deficiency), and conjugated hyperbilirubinemia (if other pituitary hormone deficiencies present).

differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with Growth Hormone Deficiency

A
  1. anterior pituitary gland
  2. somatostatin
  3. Growth hormone
  4. deficiency
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3
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with Disproportionate Short Stature

A

.

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4
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with Syndromic (Down, Turner, Prader-Willi, Noonan) Short Stature

A

.

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5
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with Psychosocial Short Stature

A

.

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6
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with a Tall Stature Disorder

A

.

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7
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with HYPOTHYROIDISM (CONGENITAL & ACQUIRED)

A

.

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8
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with THYROIDITIS

A

.

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9
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with HYPERTHYROIDISM

A

.

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10
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with THYROID CANCER

A

.

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11
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with T1D

A

.

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12
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with T2D

A

.

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13
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with Monogenic Diabetes

A

.

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14
Q

epidemiology, clinical presentation, pathophysiology, differential diagnoses, evaluation, and prognosis of a newborn, infant, child or adolescent with CF-related DM

A

.

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15
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with GHD

A

.

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16
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with DSS

A

.

17
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with SSS (Down, Turner, Noonan, Prader-Willi)

A

.

18
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with PSS

A

.

19
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with TSD

A

.

20
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with Hypothyroidism

A

.

21
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with Thyroiditis

A

.

22
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with Hyperthyroidism

A

.

23
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with Thyroid Cancer

A

.

24
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with T1D

A

.

25
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with T2D

A

.

26
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with monogenic diabetes

A

.

27
Q

best practice standards of primary health care and management of newborns, infants, children and adolescents with CF-related diabetes

A

.

28
Q

primary care pediatric nurse practitioners role in the management, support, and referral processes for children with a chronic illness/disease

A

.

29
Q

Children with … typically have normal birth weight and length. In the first 2 years of life, their linear growth velocity decelerates as they near their genetically determined percentile. After this deceleration, the child’s linear growth will be parallel to the growth curve.

A

Familial short stature

30
Q

Children with -1- do not necessarily have short parents but have a growth pattern similar to those with -2- with a decline in linear growth velocity between ages 2 and 3 years. Subsequently, the child will have normal linear growth parallel to the growth curve; however, skeletal maturation and the onset of puberty are delayed. Growth continues beyond the time the average child has stopped growing, and final height is appropriate for target height.

A
  1. constitutional growth delay

2. familial short stature

31
Q

SGA/IUGR

A

.

32
Q

The ADA and the International Society of Pediatric and Adolescent Diabetes recommend testing any youth who is -1- beginning at -2- and/or -3-, whichever is earlier, and who has 1 or more of the following additional risk factors (8)(9): 1) history of -4- or preexisting diabetes mellitus -5-, …

A
  1. overweight (defined as a BMI ≥85th percentile for age and sex) or obese (BMI ≥95th percentile for age and sex)
  2. age 10 years
  3. puberty onset
  4. maternal gestational
  5. during the pregnancy
33
Q

…2) history of being -1- age, 3) member of a high-risk -2- group, 4) family history of T2D in a -3- degree relative, 5) signs of -4-, and 6) previously diagnosed as having a condition -5-

A
  1. small for gestational
  2. racial or ethnic (Asian, Native American, Pacific Islander, Hispanic, or African ancestry)
  3. first- or second-
  4. IR (usually acanthosis nigricans)
  5. associated with IR (including central adiposity, polycystic ovary syndrome, dyslipidemia, or hypertension).
34
Q

-1- of T2D may or may not be a helpful guide because many children with T1D may also have a -1- of T2D. Thus, measurement of -2- is usually important in the differential diagnosis

A
  1. Family history

2. diabetes autoantibodies

35
Q

Acanthosis nigricans is a dermatologic marker of -1-often seen in children with -2- because of IR.

A
  1. hyperinsulinism

2. excess insulin release

36
Q

-1- is diagnosed when the -2- is greater than 600 mg/dL (>33 mmol/L), -3- is greater than 320 mOsm/kg (>320 mmol/kg), and -4- is not significant. It can lead to severe metabolic decompensation and coma and must be treated differently from DKA because it is associated with greater -5- and greater electrolyte loss with minimal ketosis.

A
  1. Nonketotic hyperosmolar hyperglycemia
  2. blood glucose level
  3. effective plasma osmolality
  4. ketosis
  5. dehydration
37
Q

Five-year outcome data in adolescents versus adults who underwent bariatric surgery in the Teen-LABS and the related adult LABS cohort studies found that adolescents sustained a -1- weight loss compared with adults that was maintained at 5 years but were -2- than adults to have sustained remission of T2D and -3-.

A
  1. similar degree (26% vs 29%) of
  2. significantly more likely (86% vs 53% & 68% vs 41%)
  3. hypertension