23 results
diagnosis management pathophysiology neurology pediatrics differential disease abnormal genetics malignant ophthalmology physicalexam pleural sclerosis shock syndrome 21hydroxylasedeficiency 21ohd agammaglobulinemia amyotrophic
Clinical features of shock from dehydration in an infant Decreased level of consciousness Sunken fontanelle Dry mucous
Clinical features ... in an infant Decreased ... #PhysicalExam #Signs ... #Symptoms #Shock ... #Dehydration #Peds
Spinal Cord Disorders - Differential Diagnosis Framework Spinal cord neurological lesion: Clinical findings: • Symptoms and signs below
neurological lesion: Clinical ... findings: • Symptoms ... and signs below ... Cauda equina- decreased ... differential #algorithm
Prader-Willi Syndrome: Pathogenesis and clinical findings • Maternal uniparental disomy: inheriting 2 copies of maternal chromosome
Pathogenesis and clinical ... Prader-Willi Syndrome Signs ... /Symptoms/Complications ... , sleep apnea, cor ... pathophysiology #peds
Amyotrophic Lateral Sclerosis (ALS) Summary ALS: combination of the clinical examination finding of amyotrophy with the pathologic
of the clinical ... cellular function Clinical ... multiple spinal cord ... fasciculations Common Symptoms ... - Fatigue and decreased
Retinoblastoma: Pathogenesis and clinical findings • Sporadic mutation -> One allele of RB1 tumor suppressor gene
Pathogenesis and clinical ... gene mutated in all ... Retinoblastoma Signs ... accumulation - Decreased ... #symptoms
Multiple Sclerosis - Summary Multiple Sclerosis (MS) is an autoimmune-mediated neurodegenerative disease of the central nervous system
cognitive impairment, decreased ... syndromes such as ... Signs and symptoms ... stimulation Clinical ... Progressive MS (Spinal cord
Pott's Disease in Tuberculosis - Diagnosis and Management Summary Epidemiology: - Typically from TB endemic areas -
extrapulmonary cases Clinical ... Signs/Symptoms: ... years - May have signs ... pain, numbness, decreased ... should be done in ALL
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Pathogenesis and Clinical ... • This is also ... Signs/Symptoms/Complications ... Late (shock): cold ... endocrinology #peds
Abnormal liver function tests algorithm. This figure details the initial response to abnormal liver blood tests.
function tests algorithm ... evaluation of the clinical ... /or suspicious clinical ... symptoms/signs ... LFTs #Abnormal #Algorithm
Aphasia - Pathophysiology and Clinical Findings Broca's Aphasia - Expressive language impairment: non-Fluent - Sensory speech areas
Pathophysiology and Clinical ... motor areas is also ... areas → Errors in word ... Pathophysiology #diagnosis #signs ... #symptoms #Brocas
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