16 results
Positive Babinski Reflex with dorsiflexion of the big toe after stroking the sole of the foot.
This
infants and usually ... Upgoing #Positive #Peds ... #Pediatrics #Clinical ... #Video #PhysicalExam ... #Primitive #pyramidal
Clinical features of shock from dehydration in an infant

Decreased level of consciousness 
Sunken fontanelle 
Dry mucous
Clinical features ... Extremities #PhysicalExam ... #Signs #Symptoms ... #Dehydration #Peds ... #Pediatrics
Asymmetrical Tonic Neck Reflex (ATNR)

This primitive reflex found in newborn babies that normally vanishes around 4
position of the infant's ... #Neck #Reflex #PhysicalExam ... #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal
The infant with tachypnea or wheeze - Clinical Conditions to Consider
 - Bronchiolitis 
 - Pneumonia
The infant with ... tachypnea or wheeze - Clinical ... disorder - Other causes ... #Diagnosis #Peds ... #Pediatrics #Infant
Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
Clinical Findings ... myoclonic seizure, primitive ... pathophysiology #geriatrics ... #diagnosis #signs ... #symptoms
Moro Reflex on Newborn Physical Exam

The Moro reflex is obtained by holding the baby’s head and
midline with the hand ... #Moro #Reflex #Peds ... #Pediatrics #Clinical ... Neurology #Normal #PhysicalExam ... #Primitive
Primitive Suck, Rooting Reflex on Newborn Physical Exam 
The normal response to stroking the lateral aspect
Primitive Suck, ... normal in the infant ... Reflex #Newborn #PhysicalExam ... #clinical #video ... #peds #pediatrics
Galant Reflex on Physical Exam

The Galant reflex is present at birth and remains until the 2nd
Galant #Reflex #PhysicalExam ... #clinical #video ... #Neurology #Peds ... #Pediatrics #Normal ... #Primitive
Grasp Primitive Reflex on Newborn Physical Exam 

Placement of the examiner’s finger in the palm of
Grasp Primitive ... causes a hand opening ... Reflex #Newborn #PhysicalExam ... #clinical #video ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Clinical Findings ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... endocrinology #peds ... #pediatrics