24 results
Primary hypoadrenalism (Addison’s disease) – symptoms, signs

#Diagnosis #Hypoadrenalism #Addisons #Disease #Hypoadrenalism #Signs #Symptoms

** GrepMed Recommended Text:
disease) – symptoms, signs ... Hypoadrenalism #Addisons ... Hypoadrenalism #Signs ... Basic and Clinical Endocrinology
Infographic depicting the main pearls of various types of congenital adrenal hyperplasia for the medical student.
of congenital adrenal ... diagnosis #comparison #treatment ... #Peds #Endocrinology ... #Adrenal #pathophysiology
Primary Adrenal Insufficiency
Addison's Disease - Damage of the adrenal glands with lack of cortisol, androgens and
vomiting • Fatigue Signs ... Reduced libido • Signs ... insufficiency #addisons ... #disease #endocrinology ... #diagnosis #signs
CLINICAL MANIFESTATIONS 
OF ADRENAL INSUFFICIENCY. 

Primary and secondary adrenal insufficiency:
 - Tiredness, weakness, mental depression
MANIFESTATIONS OF ADRENAL ... and secondary adrenal ... Insufficiency #Signs ... #Symptoms #Adrenal ... Insufficiency #Addisons
Congenital Adrenal Hyperplasia - 21-Hydroxylase Deficiency - Signs and Symptoms
 • Brain: Androgenization effects, Glucocorticoid effects,
Congenital Adrenal ... Hydroxylase Deficiency - Signs ... resistance • Adrenal ... Hydroxylase #Deficiency #Signs ... Symptoms #diagnosis #endocrinology
Suspected Celiac Disease - Diagnosis Algorithm

Celiac disease suspected:
 • Signs and symptoms of celiac disease
 •
suspected: • Signs ... unresponsive to treatment ... discernable cause • Signs ... hepatitis, T1DM, Addisons
Anastrozole is a Selective non-steroidal aromatase Inhibitor. Used for the treatment of breast cancer in postmenopausal
Used for the treatment ... which converts adrenal ... on formation of adrenal ... druginformation #treatment ... #endocrinology
Short Stature - Differential Diagnosis Algorithm
Normal Variant, Normal Puberty Onset (BA = CA)
 • Familial Short
• Congenital Adrenal ... Panhypopituitarism Treatment ... Celiac, IBD) • Renal ... Diagnosis #Algorithm #endocrinology
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
21-OHD in the adrenal ... as "congenital adrenal ... Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology
Hyperthyroidism Overview

Clinical Manifestation of Hyperthyroidism:
 • Fatigue
 • Weight loss
 • Heat intolerance
 • Depression, nervousness
↑ AST/ALT • Treatment ... tenderness Treatment ... #differential #endocrinology ... #signs #symptoms