Order EDA Gene Deletion/Duplication Test for X-Linked Hypohidrotic Ectodermal Dysplasia
X-Linked Hypohidrotic Ectodermal Dysplasia (XLHED) is characterized by three cardinal features: hypotrichosis (sparse hair), hypohidrosis (reduced sweating) and hypodontia (absence of teeth). X-linked hypohidrotic ectodermal dysplasia is inherited in an X-linked manner and caused my variants in the EDA gene. Read more details about this test.
All samples must be accompanied with a completed requisition form. Please make sure any identifiers used on the specimen is provided on the paperwork. Consent page should be signed by a health care provider. Any incomplete or missing paperwork may delay the start of testing.
Multiplex Ligation-dependent Probe Amplification (MLPA)
7ml of whole blood (3–5ml for an infant) in a lavender top tube (K2EDTA or K3EDTA)
The Laboratory for Molecular Medicine offers several billing options for our clients and their patients; however, we do not bill insurance companies and are unable to begin testing without accurate billing information.
For questions, please contact us at 617-768-8500 or by email.