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Medical genetics / Pancreas disorders / Pediatrics / Channelopathy / Cystic fibrosis / Sweat test / Congenital absence of the vas deferens / Point mutation / Genetic testing / Biology / Health / Medicine


1216 Consultation Protocol to guide the assessment of testing for hereditary mutations in the Cystic Fibrosis conductance Transmembrane Regulator (CFTR) gene February 2014
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Document Date: 2014-11-19 23:54:21

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Company

IVD / 11 Delivery / /

Country

Turkey / Australia / Denmark / /

Event

Product Issues / /

Facility

Laboratory Accreditation Standards / Royal College of Pathologists / University of Adelaide / /

IndustryTerm

carrier frequency / diagnostic medical device / healthcare resources / draft protocol / final protocol / clinical management / genetic counselling services / state-wide genetics services / diagnostic medical devices / /

MedicalCondition

infertility / chronic bacterial infection / hereditary mutations / disease / Progressive respiratory disease / common autosomal recessive disorder / idiopathic pancreatitis / established inherited disorder / less severe disease / pancreatic insufficiency / diseases / severe lung disease / disorder / cystic fibrosis transmembrane conductance regulator / Cystic Fibrosis / chronic pulmonary infections / CFTR-related disorders / progressive lung disease / disorders / late onset pulmonary disease / /

MedicalTreatment

counselling / /

Organization

University of Adelaide / Royal College of Pathologists of Australasia / National Pathology Accreditation Advisory Council / Therapeutic Goods Administration / School of Population Health / Pathology Services Table Committee / Department of Health / Medical Services Advisory Committee / National Association of Testing Authorities / Medicare / /

Position

Commonwealth Minister / Government Health Minister / /

Product

Classic Classic Television / stability / chloride conductance / premature degradation Disordered regulation / protein maturation / /

RadioStation

CFTR / /

Technology

draft protocol / diagnostic tests / ultrasound / 1216 Consultation Protocol / genotype / final protocol / /

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