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Endocrine System Diseases and Disorders. Gigantism  hyper GH before 25  extreme skeletal size.

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Presentation on theme: "Endocrine System Diseases and Disorders. Gigantism  hyper GH before 25  extreme skeletal size."— Presentation transcript:

1 Endocrine System Diseases and Disorders

2 Gigantism  hyper GH before 25  extreme skeletal size

3 Acromegaly  hyper GH during adulthood  gradual enlargement or elongation of facial bones and extremities

4 Pituitary Dwarfism Hypo GH before 25 aka proportional dwarfism Usually normal mental & sexual functions

5 Cushing syndrome  hyper glucocorticoids like cortisol  fat deposits on upper back; striated pad of fat on chest and abdomen; “moon” face  may be caused by tumor of Ant. Pit (increased ACTH)  different form may be caused by hyper aldosterone (low K)

6 Hyperthyroidism  hyper thyroid hormone  nervous, tremor, weight loss, excessive hunger; fatigue; irritability

7 Graves disease  hyper thyroid hormone  inherited or possibly autoimmune  weight loss, nervousness, increased heart rate, esophthalmos goiter

8 Hypothyroidism  hypo thyroid hormone  sluggish, weight gain; slowing of body function

9 Cretinism  hypo thyroid hormone during early development  aka deformed dwarfism  retarded mental development; facial puffiness; lack of muscle coordination

10 Goiter  lack of iodine in diet  enlargement of thyroid

11 Winter depression  hyper melatonin  Usually in winter when days are shorter (sunlight inhibits melatonin)  Aka Seasonal affective disorder (SAD)  sadness resulting from exaggerated melatonin effects  expose to high-intensity light

12 Diabetes insipidus  hypo or insensitivity to ADH  decrease in kidney’s retention of water  excessive urination  excessive thirst

13 Diabetes Mellitus “pass through honey” Insulin allows glucose to transfer into cell Hypo insulin OR target cell insensitivity to insulin Hyperglycemia  glycosuria  polyuria  polydipsia Hyperglycemia  no glucose for energy  polyphagia & use of protein & fat  ketoacidosis

14 Type I diabetes  hypo insulin due to destruction of B cells in pancreas  Inherited  sudden childhood onset  polydipsia, polyuria, weight loss, fatigue  Daily insulin injections  Aka insulin dependent daibetes mellitus (IDDM)

15 Type II diabetes  insensitivity to insulin or decreased production  slow adulthood onset;  genetic and environmental factors  polydispia, polyuria, overeating, fatigue  Non-insulin dependent (NIDDM)  Lifestyle change or oral hypoglycemic agents


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