15 results
Floppy Baby Syndrome
 • Infantile Botulism
 • Acute Flaccid Myelitis
 • Guillain Barre
 • Neonatal Myasthenia
Infantile Botulism ... Myasthenia Gravis Clinical ... LMN signs - Assess ... tone, resistance, reflexes ... #Syndrome #pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... > Neonatal and infantile ... Syndrome #genetics #pathophysiology ... #peds #pediatrics
Alzheimer’s Disease: Pathogenesis and Clinical Findings
Risk factor for Late Onset Alzheimer's (99% of cases):
 - Increasing
Pathogenesis and Clinical ... chromosome 21) Signs ... seizure, primitive reflexes ... AlzheimersDisease #Dementia #pathophysiology ... #geriatrics #diagnosis
Galant Reflex on Physical Exam

The Galant reflex is present at birth and remains until the 2nd
persistence prevents the baby ... persistent in cases ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
Landau's Reaction (Reflex)  on Physical Exam

Landau's reaction is investigated holding the baby firmly under the
Landau's Reaction (Reflex ... investigated holding the baby ... #PhysicalExam #clinical ... #video #Neurology ... #Peds #Pediatrics
Brudzinski’s Sign in Meningitis (first described in 19th century by Dr. Josef Brudzinski)

Brudzinski's sign is characterized
Passive neck flexion causes ... While the pathophysiology ... an involuntary reflex ... #Meningitis #Clinical ... #PhysicalExam #Pediatrics
Grasp Primitive Reflex on Newborn Physical Exam 

Placement of the examiner’s finger in the palm of
the foot will cause ... back of the hand causes ... happen with the baby ... #PhysicalExam #clinical ... #video #peds #pediatrics
Gowers' Sign on Physical Exam

Caused by proximal muscle weakness typically seen in muscular dystrophy

#Gowers #Sign #PhysicalExam
Gowers' Sign on ... Physical Exam Caused ... #PhysicalExam #neurology ... #clinical #video ... #pediatrics #muscular
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... enzyme 21-OHase causes ... Signs/Symptoms/Complications ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... endocrinology #peds #pediatrics
Newborn Infant - Routine Examination

Birthweight, gestational age and birthweight percentile are noted.
General observation Of the baby's
The baby must be ... is also a late sign ... This reflex is not ... the abdomen, the liver ... Examination #Peds #Pediatrics