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A 145common146 disease presents Recurrent setbacks31are Mito A 145common146 disease presents Recurrent setbacks31are Mito

A 145common146 disease presents Recurrent setbacks31are Mito - PDF document

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Uploaded On 2021-06-13

A 145common146 disease presents Recurrent setbacks31are Mito - PPT Presentation

Weakness hypotonia cramping Hypoglycaemia unexplained liver failure Proximal renal tubular wasting resulting in loss of protein magnesium phosphorous calcium and other electrolytes aminoacidu ID: 841043

146 mito loss disease mito 146 disease loss mitochondrial 145 function mitoaction immune weakness failure www org content saatchi

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1 A ‘common’ disease presents Re
A ‘common’ disease presents Recurrent setbacks/are Mito is the most common inherited form of metabolic disease. It is caused by genetic mutations that disrupt the As a result, people with mito may experience profound and prolonged fatigue, as well as worsening of existing and/or any ‘red ag’ Weakness, hypotonia, cramping, Hypoglycaemia, unexplained liver failure, Proximal renal tubular wasting resulting in loss of protein, magnesium, phosphorous, calcium and other electrolytes, aminoaciduria, WPW), cardiomyopathy.PANCREASDiabetes and exocrine pancreatic failure Gastro-oesophageal reux, delayed gastric emptying, constipation, pseudo-obstruction, chronic or recurrent vomiting.SYSTEMIC – WHOLE BODYintermittent air hunger, hypersensitive BRAIN & NERVESDevelopmental delays, mental retardation/regression, focal neurological decits , dementia, seizures , coma, neuro-psychiatric disturbances, atypical cerebral palsy, myoclonus, movement disorders, ataxia, migraines, strokes, weakness (which may be intermittent), neuropathies, absent reexes, fainting, absent or excessive sweating resulting EARSHearing loss and deafness, sensorineural hearing loss . MAYBEIT’SMITO MAY

2 BEIT’SMITO anysymptomanyorgananyage
BEIT’SMITO anysymptomanyorgananyage EYESVisual loss/blindness, optic atrophy, ptosis , retinal degeneration with signs of night blindness, colour-vision and pepper’ retinopathy . Recognising mitochondrial disease in primary care ery effort content of this publication is entirely at your own risk, and the Mito Foundation accepts no liability whatsoever for any injury, loss or damage suffered or incurred by your use of, or reliance on, the information provided in this publication. AMDF0002. Date of preparation: July 2018. Naviaux RK. A Primary Care Physician’s Guide. the Spectrum of Mitoaction. Immune function and mitochondrial disease. Available at: www.mitoaction.org/blog/immune-function-and-mitochondrial-disease. Accessed: 26 June 2018.This content was produced by Saatchi & Saatchi Wellness in Visit www.mito.org.au for more information or to nd a specialist. INCORPORATED AS GPs have an important roleto play in piecing together adiagnosis of mito.personal and familyhistory and a fullsystems reviewinvestigations to conrm any mito, receiving a rapid patient’s outcomes.the physical symptoms of mito. If mito is still suspected following investigation in Piecing together a diagnosis of mito