11 results
Pathophysiology and Effects of Insulin Deficiency

#Insulin #Deficiency #DKA #Ketoacidosis #Diabetes #Pathophysiology #Endocrinology
Pathophysiology ... Effects of Insulin Deficiency ... #Insulin #Deficiency ... Ketoacidosis #Diabetes #Pathophysiology ... #Endocrinology
Adrenal Insufficiency - Differential Diagnosis Workup Algorithm
Primary Adrenal Insufficiency:
 • Autoimmune primary adrenal insufficiency
 • Adrenoleukodystrophy,
Differential Diagnosis Workup ... Isolated ACTH-deficiency ... pituitary hormone deficiency ... Differential #Diagnosis #Workup ... #Algorithm #endocrinology
Pathogenesis of Diabetic Ketoacidosis - Insulin deficiency or severe insulin insensitivity 

#DKA #Pathophysiology #Endocrinology #Diabetes #Ketoacidosis
Ketoacidosis - Insulin deficiency ... insensitivity #DKA #Pathophysiology ... #Endocrinology
Diabetes Pathophysiology and Medication Targets

The ominous octet is one concept that summarizes the different pathophysiologic pathways
Diabetes Pathophysiology ... the different pathophysiologic ... ominous octet it works ... #Diabetes #Pathophysiology ... Targets #Drug #Endocrinology
Pathogenesis and Pathophysiology of Diabetic Ketoacidosis (DKA)

DKA is a result of an absolute or relative insulin
Pathogenesis and Pathophysiology ... relative insulin deficiency ... details of the pathophysiology ... #Pathophysiology ... DKA #Diabetes #Endocrinology
Feedback Loop: Growth Hormone (GH)
Growth Hormone:
 • Liver -> GHR activates JAK-STAT pathway -> Incr IGF1
Symptoms: • GH deficiency ... #FeedbackLoop #endocrinology ... #pathophysiology
Hypothyroid Myopathy
Very common (up to 80% ) in patients with hypothyroidism
Pathophysiology:
 • T4 deficiency leads to
hypothyroidism Pathophysiology ... : • T4 deficiency ... Hypothyroid #Myopathy #pathophysiology ... signs #symptoms #endocrinology
Thyroid Function Pathway 

Hypothyroidism is a very common condition! Here's a repost of the pathway that
pathway that is deficient ... Thyroid #Pathway #Pathophysiology ... #Endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-Hydroxylase Deficiency ... amount of enzyme deficiency ... #21HydroxylaseDeficiency #21OHD #pathophysiology ... #genetics #endocrinology
Acromegaly - Diagnosis and Management Summary - GrepMed Handbook 

Clinical Presentation: 
 • Classic Acromegaly: frontal
malignancy Pathophysiology ... Diagnosis and Workup ... Diagnosis #Management #Endocrinology ... #Treatment #Pathophysiology