15 results
diagnosis differential pediatrics neurology causes infant management pathophysiology physicalexam syndrome 21hydroxylasedeficiency 21ohd abnormal anemia atlas beaus clinical dehydration developmentaldelay disease
Causes of Developmental Delay - Differential Diagnosis Algorithm Isolated Domain Delay - Reduced Respiratory Drive: • Cognitive
Differential Diagnosis Algorithm ... Syndromic • Genetic ... Disorder (e.g. ... Differential #Diagnosis #Algorithm ... #Causes #Peds #
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
in an infant Decreased ... urine output Cold ... #PhysicalExam #Signs ... #Dehydration #Peds
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
Spinal Cord Disorders ... • Symptoms and signs ... Cauda equina- decreased ... #spinalcord #disorders ... differential #algorithm
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Prader-Willi Syndrome Signs ... , sleep apnea, cor ... PraderWilli #Syndrome #genetics ... pathophysiology #peds
Causes of Hypotonic Infant (Floppy Newborn) - Differential Diagnosis Algorithm Central Nervous System - Decreased LOC, Axial
Differential Diagnosis Algorithm ... Nervous System - Decreased ... Syndromes - Spinal Cord ... • Central Core ... #Causes #Peds #
Transverse Myelitis Overview Focal inflammatory disorder of the spinal cord resulting in rapid onset of weakness, sensory
Focal inflammatory disorder ... - Reflexes: decreased ... • Bilateral signs ... , MOG antibody disorders ... (MOG) antibody disorders
Hemolytic Anemia - Differential Diagnosis Algorithm • Sickle cells - Consider sickle cell disease (diverse genotypes):
Differential Diagnosis Algorithm ... without platelet decrease ... Agglutination - Cold ... Consider RBC membrane disorder ... Differential #Diagnosis #Algorithm
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... Late (shock): cold ... pathophysiology #genetics ... endocrinology #peds
Weakness - Differential Diagnosis Framework Approach To Weakness: • Non-neuromuscular disorder (Cardiac, pulmonary etc) • CNS ->
Non-neuromuscular disorder ... of the spinal cord ... Lack of UMN/LMN signs ... • Inflammatory disorders ... Malignancy-associated myositis • Genetic
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
cognitive impairment, decreased ... • Lhermitte’s sign ... impairment, Mood disorder ... Signs and symptoms ... Progressive MS (Spinal cord
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