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hematology hemophagocytic hlh lymphohistiocytosis pathophysiology 21hydroxylasedeficiency 21ohd anemia aplastic ascorbicacid bronchiolitis cardiology cardiomyopathy encephalopathy endocrinology hemeonc neurology nutrition oncology peripartum
Bronchiolitis Bronchiolitis is a viral inflamation of the bronchioles and the commonest LRTI in under 1s'. It's
symptoms for 1 ... REMEMBER - infants ... Bronchiolitis #pediatrics ... #diagnosis #management ... #peds #treatment
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 ... pathophysiology #genetics ... endocrinology #peds ... #pediatrics
Hemophagocytic Lymphohistiocytosis (HLH) Definition: Overwhelming clinical syndrome associated with excessive macrophage activation and cytokine storm due to
: Overwhelming clinical ... frequently affects infants ... HLH signs and symptoms ... Diagnosis via genetic ... #management #treatment
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
and Management ... eating habits • Infants ... poor nutrition Clinical ... , or any other cause ... vasculitis Treatment
Posterior Reversible Encephalopathy Syndrome (PRES) Overview Clinico-Radiological Syndrome, characterized by: • Headache • Seizures • Altered mental
Neurological symptoms ... the underlying cause ... • Treatment of ... until cause identified ... #management #neurology
Peripartum Cardiomyopathy - Summary 1. Definition • Towards the end of pregnancy to 5 months postpartum
exclude other causes ... Genetic predisposition ... Clinical • Under-recognized ... teratogenic GDMT meds ... #treatment
Aplastic Anemia - Overview Who? • M = F • 3 peaks: 1) Childhood 2) 15-25 years 3) >60 years What? • Aplastic anemia
Aplastic Anemia Clinical ... and petechiae Causes ... Syndromes: - Genetic ... • Improve the symptoms ... #management
Hemophagocytic Lymphohistiocytosis (HLH) High mortality without prompt recognition and management. HLH is a critical diagnostic consideration in
hyperinflammatory syndrome caused ... Familial) HLH: - Genetic ... Onset: Usually in infancy ... Clinical Presentation ... Common Signs and Symptoms
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