Neurology Flashcards
what is the MC chromosomal disorder and cause of mental developmental disability
trisomy 21
common findings in trisomy 21
prominent epicanthal folds (monolid)
brush field spots - white, grey or brown spots on the iris
transverse, singular palmar crease (simian crease)
AV septal defects
prenatal screening for trisomy 21 and findings
biochemical screening - first trimester; low PAPP-A
nuchal translucency US - 10-13 weeks; increased nuchal fold thickness –> chorionic villus sampling or amniocentesis should be performed
MCC meningitis in adults
strep pneumo
MCC meningitis in kids
Neisseria menigitidis
meningitis in kids is associated w
a petechial rash on trunks, legs, conjunctiva
MCC meningitis in neonates
GBS
sx meningitis
fever, HA, neck stiffness, photosensitivity
brudzinski vs kernig sign
brudzinski - neck flexion produces knee or hip flexion
kernig - inability to extend knee with hip flexion
dx meningitis
Bacterial = LP + CSF exam - decreased glucose + increased neutrophils, increased protein
Viral = LP + CSF exam - normal glucose + normal or elevated protein, increased lymphocytes
Head CT before LP
tx meningitis
cef + vanc
can use dexamethasone too
PEP for meningitis
Cipro or rifampin
droplet precautions x 24 hours after starting abx
Turner’s syndrome results from
the absence of one complete set of genes located on the X chromosome or a nonfunctioning X chromosome (45 XO)
common sx in turner’s syndrome
hypogonadism - gonadal dysgenesis (streaked ovaries), absence of breasts, infertility
CV - coarctation of art, bicuspid aortic valve
PE for turner’s syndrome
short stature
webbed neck
broad chest with widely spaced nipples “shield chest”