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management treatment 21hydroxylasedeficiency 21ohd acromegaly adrenal algorithm anxiety ascorbicacid behavioraldisorder cah comparison congenitaladrenalhyperplasia examination newborn nutrition panicdisorder physicalexam psychiatry scurvy
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
CAH #algorithm #causes ... #diagnosis #comparison ... #treatment #Peds ... #Endocrinology ... #Adrenal #pathophysiology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
enzyme 21-OHase causes ... deficiencies present in infants ... Signs/Symptoms/Complications ... #genetics #endocrinology ... #peds #pediatrics
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook Clinical Presentation: • Classic Acromegaly: frontal
malignancy Pathophysiology ... phenytoin, minoxidil), genetic ... or refractory cases ... #Management #Endocrinology ... #Treatment #Pathophysiology
Panic Disorder: Pathogenesis and clinical findings Social Factors • Parenting and infant attachment • Childhood illness/abuse •
Parenting and infant ... Neurotic personality Genetics ... sweating, trembling, nausea ... BehavioralDisorder #Pathophysiology ... #diagnosis #symptoms
Scurvy (Vitamin C Deficiency) - Diagnosis and Management Vitamin C is required for hydroxylation of proline residues
Deficiency) - Diagnosis ... eating habits • Infants ... Psychiatric symptoms ... nonimmune hemolysis MSK ... , or any other cause
Newborn Infant - Routine Examination Birthweight, gestational age and birthweight percentile are noted. General observation Of the baby's
Newborn Infant - ... When the diagnosis ... paediatrician or geneticist ... #Examination #Peds ... #Pediatrics #Diagnosis
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