Peds1 Flashcards
Why is acute bacterial sinusitis so common after a viral URI?
Swelling of nasal turbinates and mucosa allow for secondary bacterial infection because contaminated bacteria can’t be cleared (due to mucosal inflammation).
Rx = Amoxicillin + clavulanic acid
Symmetric arthritis in > 1 joint with mild erythema and warmth at joints in a child without rash or fever.
Juvenile Idiopathic Arthritis. Symmetric arthritis for at least 6 weeks. Systemic inflammation with possible inflammatory markers (ESR, CRP), hyperferritinemia, hypergammaglobulinemia, and thrombocytosis.
Anemia is common due to chronic inflammation and iron deficiency and improves with MTX.
Young girl with normal development followed by progressive loss of speech, loss of purposeful hand use, gait disturbance, stereotypical hand movements, and head growth deceleration:
Rett Syndrome. Mostly girls. Seizures common and increase with age. Due to mut in X linked MECP2 gene.
Fever, inspiratory stridor, barking cough:
Croup/Laryngotracheobronchitis due to Parainfluenza
First line Rx for pertussis:
Macrolides
Teen with facial puffiness, fatigue, decreased appetite, periorbital and pretibial edema and recent HepB infection. 4+ protein in urine, no RBC/casts. Dx?
Membranous nephropathy (assoc with HepB)
Congenital Adrenal Hyperplasia is due to deficiency of:
21a-hydroxylase. Newborn screening with elevated 17 hydroxyprogesterone confirms Dx. Presents as HoTN and hyper K (low aldosterone) and virilization (high testosterone)
Conjunctival injection, pale follicles, tarsal inflammation, and thickened conjunctiva in a child in high populated area:
Trachoma. Due to C trachomatis (leading cause of blindness worldwide). Look for low socioeconomic areas. Active phase characterized by follicular conjunctivitis and pannus (neovascularization) formation in cornea. Rx = Azithro
Rx for impetigo:
Mupirocin if local/limited.
Cephalexin, dicloxacillin, or clinda if extensive.
Definitive diagnostic test for phenylketonuria:
Quantitative AA analysis.
Mut in Phenylketonuria:
AR mutation»_space; deficiency of phenylalanine hydroxylase, normally responsible for converting phenylalanine»_space; tyrosine.
Enzyme def in fructose metabolism disorder:
Aldolase B is deficient in hereditary fructose intolerance.
Atresia of the jejunum or ileum is thought to be due to ___ in utero
vascular accident (due to maternal cocaine use)
Enzyme deficient in angular chelitis, glossitis (hyperemic tongue), stomatitis (hyperemic oropharyngeal mucous membrane), normocytic anemia, and seborrheic dermatitis:
B2 (riboflavin). Found in dairy, eggs, meat, veggies
Enzyme deficient in dermatitis, glossitis, diarrhea, dementia:
B3 (Niacin)