23 results
Practical Pediatric Viral Rash Algorithm

Child presenting with rash and current/ recent symptoms of viral illness but
Practical Pediatric ... Viral Rash Algorithm ... five days and no signs ... #Pediatrics #Peds ... #Diagnosis
Prader-Willi Syndrome: Pathogenesis and clinical findings
 • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... delayed puberty -> Infertility ... pathophysiology #peds ... #pediatrics
Dermatofibroma 
 - Skin-colored to brown papule or nodule 
 - Firm, indurated texture 
 -
Male - Dimple sign ... Dermatofibroma #Dermatology ... #Diagnosis #Benign ... #Clinical #Photo
Pediatric Neutropenia Workup Algorithm

DOI: 10.1111/ijlh.13210

#Neutropenia #Workup #Algorithm #diagnosis #hematology #Pediatrics #peds
Pediatric Neutropenia ... Workup Algorithm ... Neutropenia #Workup #Algorithm ... #diagnosis #hematology ... #Pediatrics #peds
Epiglottitis - Swollen inflamed epiglottis 
Clinical (Rapid onset) 
 • Fever 
 • Sore throat
inflamed epiglottis Clinical ... #Epiglottitis #Signs ... #Causes #Diagnosis ... #Differential #Peds ... #Pediatrics
Staphylococcal Scalded Skin Syndrome (SSSS)

A 5-year-old girl presents to the ED with a rash that started
Syndrome #SSSS #Clinical ... #Photo #Peds #Pediatrics ... #Dermatology
Clinical Algorithm for Emergency Department Evaluation and Management of UTI in Febrile Infants and Young Children

Urinary
Clinical Algorithm ... do not replace clinical ... #Diagnosis #Management ... Febrile #Infant #Peds ... #UrinaryTract #Pediatrics
Clinical Features and Complications of Measles

Rash:
Spreads downwards, from behind the ears to the whole Of the
Clinical Features ... #Measles #Diagnosis ... Kopliks KoplikSpots #Peds ... #Pediatrics #Timeline ... #Signs #Symptoms
Combination of Skin Findings and Arthritis in Pediatrics Patient - Differential Diagnosis
Malar rash: 
 • A
and Arthritis in Pediatrics ... - Differential Diagnosis ... migrans: • Target sign ... gabrieltalledop #dermatology ... #peds #pediatrics
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings
Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... Signs/Symptoms/Complications ... Hirsutism & acne • Infertility ... endocrinology #peds ... #pediatrics