ANS: C
In children with hypopituitarism, the skeletal proportions are normal. Growth is within normal limits for the first year of life. Height is usually more delayed than weight. Intelligence is not affected by hypopituitarism.
ANS: B
Excess GH after the closure of the epiphyseal plates results in acromegaly. Dwarfism is the condition of being abnormally small. Gigantism occurs when there is hypersecretion of GH before the closure of the epiphyseal plates. Cretinism is associated with hypothyroidism.
ANS: C
Manifestations of sexual development before age 9 in boys and 8 in girls are considered precocious and should be investigated. However, recent research indicates that puberty is beginning early in girls and it is suggested that precocious puberty may be evident as young as 6 or 7 years of age. Boys older than 9 years of age and girls older than 8 years of age fall within the expected range of pubertal onset.
ANS: D
Precocious puberty of central origin is treated with monthly subcutaneous injections of luteinizing hormone–releasing hormone. Thyrotropin, gonadotropin, and somatotropic hormone are not appropriate therapies for precocious puberty.
ANS: B
The principal disorder of posterior pituitary hypofunction is diabetes insipidus. The anterior pituitary produces growth hormones, thyroid-stimulating hormones, adrenocorticotropic hormones, gonadotropin, prolactin, and melanocyte-stimulating hormone. The adrenal cortex produces aldosterone, sex hormones, and glucocorticoids. The adrenal medulla produces catecholamines.
ANS: D
Excessive urination accompanied by insatiable thirst is the primary clinical manifestation of diabetes. These symptoms may be so severe that the child does little other than drink and urinate. Oliguria is decreased urine production and is not associated with diabetes insipidus. Glycosuria is associated with diabetes mellitus. Nausea and vomiting are associated with inappropriate antidiuretic hormone secretion.
ANS: C
Dry skin, mental decline, and myxedematous skin changes are associated with juvenile hypothyroidism. Children with hypothyroidism are usually sleepy. Constipation is associated with hypothyroidism and decelerated growth is common.
ANS: A
A goitre is an enlargement, or hypertrophy, of the thyroid gland. Goitre is not associated with the adrenals or the anterior and posterior pituitaries.
ANS: B
Exophthalmos is manifested as protruding eyeballs and is a clinical manifestation of hyperthyroidism. Hypothyroidism, hypoparathyroidism, and hyperparathyroidism are not associated with exophthalmos.
ANS: C
Children being treated with propylthiouracil must be carefully monitored for the adverse effects of the drug. Parents must be alerted that sore throat and fever accompany the grave complication of leukopenia, so these symptoms should be immediately reported. Weight gain, episodes of ear pain, and stomach flu are not usually associated with leukopenia.
ANS: C
Vitamin D toxicity can be a serious consequence of vitamin D therapy. Parents are advised to watch for signs including weakness, fatigue, lassitude, headache, nausea, vomiting, and diarrhea. Renal impairment is manifested through polyuria, polydipsia, and nocturia. Headaches may be a sign of vitamin D toxicity, but seizures are not. Physical restlessness and a voracious appetite with weight loss are manifestations of hyperthyroidism. Anorexia and insomnia are not characteristic of vitamin D toxicity.
ANS: C
These hormones are secreted by the adrenal cortex. The thyroid gland produces thyroid hormone and thyrocalcitonin. The parathyroid glands produce parathyroid hormones. The anterior pituitary produces growth hormone, thyroid-stimulating hormone, adrenocorticotropic hormone, gonadotropin, prolactin, and melanocyte-stimulating hormone.
ANS: B
Addison’s disease is chronic adrenocortical insufficiency. Graves’ and Hashimoto’s diseases involve the thyroid gland. Cushing’s syndrome is a result of excessive circulation of free cortisol.
ANS: B
The most common biochemical defect with congenital adrenal hyperplasia is partial or complete 21-hydroxylase deficiency. With complete deficiency, insufficient amounts of aldosterone and cortisol are produced, so circulatory collapse occurs without immediate replacement. Vitamin D, stool softeners, and calcium carbonate have no role in the treatment of adrenogenital hyperplasia.
ANS: C
The onset of immune-mediated type 1 diabetes mellitus typically occurs in children or young adults. Peak incidence is between the ages of 10 and 15 years. Infrequent ketoacidosis, gradual onset, and treatment with oral agents are more consistent with type 2 diabetes.
ANS: D
Hallmarks of diabetes mellitus are glycosuria, polyuria, and polydipsia. Nausea and seizures are not clinical manifestations of diabetes mellitus. Impaired vision is a long-term complication of the disease.
DIF: Cognitive Leve
ANS: C
Blood glucose self-management has improved diabetes management and can be used successfully by children from the time of diagnosis. Insulin dosages can be adjusted on the basis of blood sugar results. Blood glucose monitoring is more expensive but provides improved management. It is as accurate as equivalent testing done in laboratories. The ability to self-test allows the child to balance diet, exercise, and insulin. The parents are partners in the process, but the child should be taught how to manage the disease.
ANS: C
Exercise lowers blood glucose levels, which can be compensated for by extra snacks. Exercise is encouraged and not restricted, unless indicated by other health conditions. Extra insulin is contraindicated because exercise decreases blood glucose levels.
ANS: D
Symptoms of hypoglycemia are treated with a rapid-releasing sugar source followed by a complex carbohydrate and protein. Saturated and unsaturated fat, fruit juice, and several glasses of water do not provide the child with the complex carbohydrates and protein necessary to stabilize the blood sugar.
ANS: D
Some of the clinical manifestations of hypoglycemia include shaky feelings; dizziness; difficulty concentrating, speaking, focusing, and coordinating; sweating; and pallor. Lethargy, thirst, nausea, and vomiting are manifestations of hyperglycemia.
ANS: B
School-age children are able to give their own injections, but parents should still participate in learning and giving the insulin injections. He is already old enough to administer his own insulin. The child is able to use thighs, abdomen, part of the hip, and arm. He can obtain assistance if he needs to use other sites.
ANS: D
The abdomen has the fastest rate of absorption but the shortest duration. The arm has a fast rate of absorption but short duration. The leg has a slow rate of absorption but a long duration. Finally, the buttock has the slowest rate of absorption and the longest duration.
ANS: A
Increased secretion of ADH causes the kidneys to resorb water, which increases fluid volume and decreases serum osmolarity, resulting in a progressive reduction in sodium concentration. The immediate management for the child is to restrict fluids. The child should also be weighed at the same time each day. Encouraging fluids, turning frequently, and maintaining nothing by mouth are not associated with SIADH.