peds104 Flashcards

1
Q

decreased IgG, IgA, IgM, and IgE, along with absent or markedly decreased B cells

A

Brutton’s agammaglobulinemia

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2
Q

onset of recurrent bacterial infections in the first 5 yr of life; serum IgG, IgM, and IgA low; absent isohemagglutinins or poor response to vaccines; less than 2percent cd19 pos B cells

A

brutton’s agammaglobulinemia

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3
Q

boy with eczema, thrombocytopenia, and recurrent infections with encapsulated germs

A

wiskott-aldrich syndrome

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4
Q

presents at birth with petechiae, bruises, bleeding from circumcision, or bloody stools

A

wiskott-aldrich

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5
Q

low IgM, high IgA and IgE; poor antibody response to polysaccharide antigens, modertely reduced T cells and platelets

A

wisott-aldrich syndrome

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6
Q

recurrent and uncontrolled infections with catalase-pos organisms

A

chronic granulomatous disease

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7
Q

lymphadenitis, and abscesses of the skin and viscera (liver); lymphocytes are normal

A

chronic granulomatous disease

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8
Q

an immediate anaphylactic reaction, an encephalopathy, or any CNS complication within 7 days of DTAP, means do what for the next dose?

A

only give DT; the acellular pertussis is prob responsible so we hold off on that

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9
Q

by age 1 yo, what should weight and height be?

A

weight should triple and height should increase by 50 percent

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10
Q

twice daily administration of prophylactic penicillin should be given to kids with sickle ceel disease until hwen

A

5 years of age

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11
Q

infant with cyanosis that is aggravated by feeding nad relieved with crying

A

choanal atresia

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12
Q

management of choanal atresia

A

place an oral airway and lavage feeding; definitive treatment is repairing the obstruction with surgery or endoscopy

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13
Q

inspiratory stridor that is exacerbated by any exertion; symptoms appear in the first 2 weeks of life an dincrease in severity

A

laryngomalacia

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14
Q

caf au lait spts, macrocephaly, feeding problems, short stature, learning disabilities

A

NF type 1

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15
Q

bilateral acoustaic neuromas and cataracts

A

NF type 2

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16
Q

fine reticular granulatiry of the lung parenchyma

A

classic in hyaline membrane disease

17
Q

chest xray shouws prominent pulmonary vascular markings,, fluid lines in the fissures, overaeration, a flat diaphragm, and occasionally pleural fluid

A

transient tachypnea of the newborn

18
Q

persistent pulm htn of the newborn

A

cyanosis; persistence of fetal circulatory pattern of R to L shunting; hypoxia unresponsive to 100percent oxygen;

19
Q

meconium aspiration can lead to pneumothorax or pneumodiastinum

A

right

20
Q

patchy infiltrates, coarse streaking of both lung fields, increased anterposteriod diameter, and flattening of the diaphrag,

A

chest xray in meconium aspiration

21
Q

osgood schlatters disease

A

aka traction apophysitis

22
Q

what bacteria is associated with infants with indwelling IV catheters

A

coag neg staph

23
Q

most common causes of early onset and late sepsis

A

GBS and E coli

24
Q

hypotonia, hepatosplenomegaly, cervical lymphadenopath, protruding abdomen, cherry red spon on macula, regression of milestones

A

niemann-pick disease