Disorders


 

SFTPB-Related Pulmonary Surfactant Metabolism Dysfunction


Synonym(s): Congenital Pulmonary Alveolar Proteinosis 1, Interstitial Lung Disease Due To Surfactant Protein B Deficiency, Pulmonary Surfactant Metabolism Dysfunction 1

 

OMIM

GeneLocusProtein
SFTPB2p12-p11.2Pulmonary surfactant-associated protein B

Laboratory Test Method Prenatal Carrier *
Ambry Genetics Corp, Ambry Genetics - Aliso Viejo, CA, USA• Sequence analysis of the entire coding region
Edith Wolfson Medical Center, Molecular Genetics Laboratory - Holon, Israel• Sequence analysis of the entire coding region
 
Gene Analysis Service - Berlin, Germany• Sequence analysis of the entire coding region
Johns Hopkins Hospital, DNA Diagnostic Laboratory - Baltimore, MD, USA• Sequence analysis of the entire coding region

* Carrier column is relevant to autosomal recessive and X-linked inheritance; column will be blank when it is not relevant (e.g. autosomal dominant inheritance, microdeletions/duplications) and/or is not offered by the lab.

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