4 results
21hydroxylasedeficiency disease endocrinology examination features hematology hemophagocytic hlh kawasaki lymphohistiocytosis management newborn pathophysiology physicalexam signs treatment
Kawasaki Disease (Mucocutaneous Lymph Node Syndrome) An rare systemic acute febrile vasculitic syndrome. Aetiology unknown. Affects
Affects children ... Early diagnosis ... Disease #Features #Signs ... #Symptoms #Diagnosis ... #Peds #Pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
deficiencies present in infants ... Signs/Symptoms/Complications ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
Overwhelming clinical syndrome ... infants < 3 months ... : HLH signs and ... symptoms can mimic ... Diagnosis via genetic
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
is also a late sign ... paediatrician or geneticist ... for any midline defects ... #Examination #Peds ... #Pediatrics #Diagnosis
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