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. 2017 Jun 19;5:121. doi: 10.3389/fped.2017.00121

Table 6.

Comparison between ME/CFS and factitious disorder/Munchausen’s syndrome by proxy/fabricated or induced illness.

Pediatric ME/CFS Factitious disorder by proxya
Prevalence Approximately 100–500 per 100,000 Very rare, approximately 0.4–2 per 100,000

Age and age range Peak age 10–17 years, range 2–17 years Average age 4 years; >50% of patients are aged <2 years; extremely rare in adolescents

Symptoms Consistent pattern of symptoms: reduction in activity, post-exertional worsening of symptoms, fatigue and loss of stamina, unrefreshing sleep, cognitive problems, orthostatic intolerance and headaches; a history of surgeries is uncommon No consistent symptoms. Most frequently reported are: apnea/cyanosis, anorexia/feeding problems, diarrhea, seizures, asthma, allergy, fevers, behavioral problems, and other sometimes bizarre symptoms, a history of surgeries is common

Clinical signs Intermittent conspicuous facial pallor, acrocyanosis, joint hypermobility common, blood pressure can fall or heart rate rise on prolonged standing No consistent clinical signs, many patients have multiple surgical scars

Orthostatic intolerance (OI) Many patients have POTS or NMH Not reported

Blood testing Routine blood tests usually normal Routine blood tests can show bizarre abnormalities

Neuroimaging Neuroimaging can reveal defects in brain perfusion and/or metabolism No reports of neuroimaging

Multiple doctors seen Common Common

Hospital admissions Hospital admissions unusual Hospital admissions very common

Medical knowledge Parents can be very knowledgeable about ME/CFS Parent/perpetrator can be knowledgeable about medical conditions

School absence Common, it is the most common medical cause of prolonged school absence Most patients are pre-school age. Common in school-age patients

Separation from parents Detrimental. Patient does not recover, illness often worsens Patient improves/recovers when separated from a parent/perpetrator

Mortality Extremely low Approximately 10% in patients and 25% in patients’ siblings

aShaw et al. (89).