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6 Cards in this Set

  • Front
  • Back
Hypopituitary dwarfism
deficiency in growth hormone in childhood; delayed puberty, appears much younger than chronological age; infantile facial features and chubbiness
Achondroplastic dwarfism
genetic disorder; normal trunk, short arms, legs and short stature.
Marfan syndrome
inherited connective tissue disorder. s/s are tall thin stature, hyperextensible joints, armspan greater than height, pubis to sole measurement > crown to pubis; sternal deformity, high arched narrow plate; early death due to cardiovascular disease such as mitral regurgitation and aortic disection.
Acromegaly(Hyperpituitarism)
excessive growth hormone after normal completion of body growth; overgrowth of bone in face, head, hands, and feet but no change in height. enlargement of internal organs: cardiomegally. metabolic disorders (dm)
Gigantism
excessive secretion of growth hormone by anteriopituitary resulting in overgrowth of entire body. The epiphyses plate does not close. increased height, weight and delayed sexual development occurs.
cushings syndrome
administration or excessive production of adrenocorticotropin (ACTH) by the pituitary will cause the adrenal cortex to secret excess cortisol; s/s : weight gain and edema with central trunk and cervical obesity and round, moon face.