
Health Dictionary
Reliable, easy-to-read patient information on common medical conditions — written in plain language, free of jargon, and grounded in current evidence. Browse the most frequent diagnoses, understand what they mean for everyday life, and learn which steps and questions help you have a focused conversation with your doctor.
Creutzfeldt-Jakob disease physical examination
Introduction
Overview
Overview
Physical Examination
Physical Examination
Appearance of the Patient
- Patients with Creutzfeldt-Jakob disease usually appear confused.
Vital Signs
- Vital Signs of patients with Creutzfeldt-Jakob disease are usually normal.
Skin
- Skin examination of patients with Creutzfeldt-Jakob disease is usually normal.
HEENT
- HEENT examination of patients with Creutzfeldt-Jakob disease is usually normal.
Neck
- Neck examination of patients with Creutzfeldt-Jakob disease is usually normal.
Lungs
- Pulmonary examination of patients with Creutzfeldt-Jakob disease is usually normal.
Heart
- Cardiovascular examination of patients with Creutzfeldt-Jakob disease is usually normal.
Abdomen
- Abdominal examination of patients with Creutzfeldt-Jakob disease is usually normal.
Back
- Back examination of patients with Creutzfeldt-Jakob disease is usually normal.
Genitourinary
- Genitourinary examination of patients with Creutzfeldt-Jakob disease is usually normal.
Neuromuscular
Physical examination of patients with Creutzfeldt-Jakob disease is usually remarkable for:[1][2][3][4][5]
- Speech impairment
- Myoclonus
- Ataxia
- Gait disturbances
- Rigid posture
- Dysarthria
- Myoclonus
- Visual changes leading to cortical blindness
- Akinetic mutism in the last stages of the disease
- Chorea
- Peripheral neuropathy
- Altered mental status
Myoclonus is the most common sign in patients Creutzfeldt-Jakob disease.
Patient is usually disoriented to persons, place, and time.
Extremities
- Extremities examination of patients with Creutzfeldt-Jakob disease is usually normal.
References
References
- ↑ Head MW, Ironside JW (June 2012). “Review: Creutzfeldt-Jakob disease: prion protein type, disease phenotype and agent strain”. Neuropathol. Appl. Neurobiol. 38 (4): 296–310. doi:10.1111/j.1365-2990.2012.01265.x. PMID 22394291.
- ↑ Argelander H (May 1968). “[The psychoanalytic dialogue]”. Psyche (Stuttg) (in German). 22 (5): 325–39. PMID 5710312.
- ↑ Sikorska B, Knight R, Ironside JW, Liberski PP (2012). “Creutzfeldt-Jakob disease”. Adv. Exp. Med. Biol. 724: 76–90. doi:10.1007/978-1-4614-0653-2_6. PMID 22411235.
- ↑ Sitammagari KK, Masood W. PMID 29939637. Missing or empty
|title=(help) - ↑ Helton AS, Snodgrass FG (September 1987). “Battering during pregnancy: intervention strategies”. Birth. 14 (3): 142–7. PMID 3689509.
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Associate Editor(s)-in-Chief: Mohamadmostafa Jahansouz M.D.[2]
