11 results
signs diagnosis peds syndrome clinical cushings genetics pathophysiology 21hydroxylasedeficiency 21ohd arm assessment chvostek cirrhosis dehydration elbow evaluation features febrile fever
The Febrile Child - some diagnostic clues to evaluating the febrile child. #Febrile #Fever #Evaluation #Assessment #Signs
Evaluation #Assessment #Signs ... #Symptoms #PhysicalExam ... Diagnosis #Peds #Pediatrics
Guide for testing and documenting neurological function in kids with upper limb fractures Rock - Median
with upper limb fractures ... Ulnar Nerve OK Sign ... #Diagnosis #Pediatrics ... Peripheral #Nerves #PhysicalExam
Cushing Syndrome - Signs and Symptoms Generalized: Weight gain, Slow healing of cuts, Increased risk of infections,
Cushing Syndrome - Signs ... and Symptoms Generalized ... Increased risk of fractures ... #Symptoms #diagnosis ... #endocrinology
The Chvostek sign (/ˈkvɒstɪk/) is a clinical sign of existing nerve hyperexcitability (tetany) seen in hypocalcemia.It
The Chvostek sign ... is a clinical sign ... level due to a shift ... #Hypocalcemia #PhysicalExam ... Video #Clinical #endocrinology
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 Hypothyroidism – symptoms and signs. Symptoms: Tiredness/malaise, Weight gain, Anorexia, Cold intolerance, Poor memory, Change in appearance, Depression, Poor libido,
Hypothyroidism – symptoms ... and signs. ... Symptoms: Tiredness ... #PhysicalExam # ... Endocrinology
Pediatric Elbow Injuries - Elbow Xrays Check the fat pads on the lateral projection: 1. A displaced anterior
Pediatric Elbow ... fat pad (sail sign ... associated with fractures ... central axis of the shaft ... Radiology #peds #Pediatrics
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Extremities #PhysicalExam ... #Signs #Symptoms ... Dehydration #Peds #Pediatrics
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... /Symptoms/Complications ... Incr Skeletal fractures ... pathophysiology #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... pathophysiology #genetics #endocrinology ... #peds #pediatrics
Cushing's Syndrome - Hypercortisolism - Diagnosis and Clinical Features 1) Skin • Thin, easily bruisable skin with
Hyperpigmentation is not a feature ... , pathological fractures ... Hypercortisolism #Diagnosis #signs ... #symptoms #endocrinology
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