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31 Cards in this Set
- Front
- Back
what is short stature what is average stature
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"average" (50th percentile) plus or minus two standard
deviations (3rd-97th percentile). Measurements that fall below the 3rd percentile for height are termed short stature. |
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Risk Factors/Etiology. there are four basic patterns of proportional short stature:
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TRisk Factors/Etiology. here are four basic patterns of proportional short stature: pathologic
(postnatal onset), constitutional growth de |
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Presentation. Pathologic short stature and constitutional short stature
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Presentation. Pathologic short stature and constitutional short stature both start out with the
patient in the normal range for height. Over time, the patient with pathologic short stature starts falling off the height curve, crossing percentiles. In constitutional short stature, normal final adult height is reached, but the growth spurt and puberty are delayed |
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familial
short stature |
familial
short stature stay parallel to the growth curve. There is a strong family history of short stature. |
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Prenatal short stature
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Prenatal short stature also is parallel to the growth curve but is much more marked
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the single most important tool in evaluating disorders of
growth. |
growth chart is the single most important tool in evaluating disorders of
growth. As many points as possible should be plotted to see trends. Physical exam is helpful in diagnosing syndromes and diseases associated with short stature. |
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Any female being evaluated
for short stature should have a |
Any female being evaluated
for short stature should have a karyotype (Turner syndrome |
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single, most important
diagnostic study in short statur is |
single, most important
diagnostic study is to obtain an x-ray of the left hand and wrist for bone age. |
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Treatment.short statur
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Treatment. Correction of the underlying disease state may help improve height. Some patients
respond to human growth hormone. |
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Differential Diagnosis.short statur
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Differential Diagnosis. Work-up for short stature.
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Tall Stature can be cause...
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Exogenous obesity can also cause
tall stature. Endocrine causes of tall stature include growth hormone excess (gigantism, acromegaly), androgen excess (tall as children but short as adults), and hyperthyroidism |
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Genetic syndromes and metabolic disorders responsible for tall stature include
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Genetic syndromes and metabolic disorders responsible for tall stature include homocystinuria,
cerebral gigantism, Beckwith-Wiedemann, Weaver-Smith, and Klinefelter syndromes. Homocystinuria is autosomal recessive, with an incidence of 1:200,000. Patients have a Marfanoid appearance with associated mental retardation or psychiatric illness. |
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Cerebral
gigantism |
Cerebral
gigantism (Sotos syndrome) are large for gestational age, have mental retardation, and a mild hydrocephalus. |
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Evaluation of Growth
Growth velocity: |
Yearly increments of growth; should follow a growth curve
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Evaluation of Growth
Chronologie age (CA): |
Actual age
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Evaluation of Growth
Bone age (BA): |
X-ray of left hand and wrist
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Evaluation of Growth
I. Ideal. |
I. Ideal. CA = BA with normal growth velocity
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Evaluation of Growth
CA >BA |
with normal growth velocity: constitutional delay
with abnormal growth velocity: chronic systemic disease, endocrine disorders |
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Evaluation of Growth CA = BA
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with normal growth velocity: genetic short stature
with abnormal growth velocity: genetic, chromosomal, syndrome |
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Evaluation of Growth
CA< BA |
with normal growth velocity: obesity
with abnormal growth velocity: precocious puberty, congenital adrenal hyperplasia (CAH), hyperthyroidism |
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DISORDERS OF WEIGHT
Failure to Thrive Definition. |
Definition. Failure to thrive is failure to gain weight or deceleration of weight growth.
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DISORDERS OF WEIGHT
Failure to Thrive Risk Factors/Etiology. |
Risk Factors/Etiology. Failure to thrive can result from malnutrition (starvation, deprivation,
abuse), malabsorption (from infection, celiac disease, cystic fibrosis, disaccharidase deficiency, protein-losing enteropathy), allergies, immune deficiency states, and chronic disease. |
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DISORDERS OF WEIGHT
Failure to Thrive Presentation. |
Presentation. Again growth charts are invaluable. In infants, birth weight is doubled by 4-5
months of age and tripled by 1 year. Patients may show little subcutaneous fat, muscle wasting, rashes, poor tone, and weak cry. |
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DISORDERS OF WEIGHT
Failure to Thrive Diagnostic Tests what .test should be considered |
Diagnostic Tests. Hospitalization for documentation of caloric intake and weight gain is sometimes
necessary. Complete blood counts, urinalysis, liver function tests, and serum protein should be drawn. A sweat chloride test should be considered |
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obesity
Definition. |
Obesity
Definition. Obesity is a generalized, excessive over-accumulation of fat. It may result from an increase in number or size of adipocytes. .. |
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obesity
Risk Factors/Etiology |
Parental obesity and family inactivity can predispose to obesity, Feeding
babies as a generic response to any crying can lead to obesit Too much fruit juice in the first year of life has been linked with subsequent obesity Some syndromes are related to obesity |
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obesity
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Presentation. Tall stature may sometimes be seen. Boys may present with increased adipose tissue
in the mammary area mistaken for breast development.Abdominal striae are present. A large pubic fat pad gives the appearance of micropenis. Puberty may come early. Associated obesity of the proximal extremities is COlIJnWIl. |
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obesity
Diagnostic Tests, |
Diagnostic Tests, Body mass index (EMl) >95% for age/sex or >30 in adolescents is used to
define obesity. |
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obesity
Treatment. |
Treatment. Exercise and a balanced diet are the keystones to effectively managing obesity.
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obesityComplications.
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Complications. Obese infants and children are at increased risk for becoming obese adults.
This is related to more advanced age of onset and severity of obesity. Complications include cardiovascular (hypertension, increased cholesterol), hyperinsulinism, slipped capital femoral epiphysis, and sleep apnea. |
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obesity dd
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Differential Diagnosis. This includes endocrine causes (Cushing, hypothyroidism, Prader..
Willi) and genetic causes (Turner, Laurence-Moon.. Biedl) , |