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  • Utah Newborn Hearing Screening & Cchd Weekly Reporting Form

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Rev 6/25/2018Utah Newborn Hearing Screening & CCHD Weekly Reporting Form Please print clearly and fill out all that applyMidwifeScreenerBaby Info Baby Name:Mom Info Moms Name:Baby DOB:Moms DOB:Gender:Phone:Blood.

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The purpose of newborn screening is to detect potentially fatal or disabling conditions in newborns as early as possible, often before the infant displays any signs or symptoms of a disease or condition.

Newborn hearing screening. All newborns in hospital and community settings will get universal hearing screening as part of the Infant Hearing Program. Hearing screening identifies infants who should have more in-depth testing for hearing loss as early as possible. Most babies will pass the newborn hearing screening.

Ideally, the test is done in the first 4 to 5 weeks, but it can be done at up to 3 months of age. If you're not offered a screening test, ask your health visitor, local audiology department or GP to arrange an appointment, or contact your local newborn hearing screening service.

IMPORTANCE OF NEWBORN SCREENING Utah State Law UCA 26-10-6 [Appendix A] requires all infants born in Utah be tested. The Utah Department of Health began managing the newborn screening process in 1979.

A newborn undergoes a hearing screening. Two different tests are used to screen for hearing loss in babies. Your baby can rest or sleep during both tests. Otoacoustic emissions (OAE) tests whether some parts of the ear respond to sound.

Babies get tested for many things right after they are born. The heel prick includes a test for phenylketonuria (PKU), a rare birth defect that causes a certain amino acid to build up in the body.

The screening tests detect disorders including metabolic, hormone, and blood disorders. Babies born with one of these disorders can appear healthy in the newborn period.

Newborn screening tests may include: Phenylketonuria (PKU). PKU is an inherited disease in which the body cannot metabolize a protein called phenylalanine. ... Congenital hypothyroidism. ... Galactosemia. ... Sickle cell disease. ... Maple syrup urine disease. ... Homocystinuria. ... Biotinidase deficiency. ... Congenital adrenal hyperplasia.

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© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232
Form Packages
Adoption
Bankruptcy
Contractors
Divorce
Home Sales
Employment
Identity Theft
Incorporation
Landlord Tenant
Living Trust
Name Change
Personal Planning
Small Business
Wills & Estates
Packages A-Z
Form Categories
Affidavits
Bankruptcy
Bill of Sale
Corporate - LLC
Divorce
Employment
Identity Theft
Internet Technology
Landlord Tenant
Living Wills
Name Change
Power of Attorney
Real Estate
Small Estates
Wills
All Forms
Forms A-Z
Form Library
Customer Service
Terms of Service
DMCA Policy
About Us
Blog
Affiliates
Contact Us
Privacy Notice
Delete My Account
Site Map
Industries
Forms in Spanish
Localized Forms
State-specific Forms
Forms Kit
Legal Guides
Real Estate Handbook
All Guides
Prepared for You
Notarize
Incorporation services
Our Customers
For Consumers
For Small Business
For Attorneys
Our Sites
US Legal Forms
USLegal
FormsPass
pdfFiller
signNow
airSlate workflows
DocHub
Instapage
Social Media
Call us now toll free:
1-877-389-0141
As seen in:
  • USA Today logo picture
  • CBC News logo picture
  • LA Times logo picture
  • The Washington Post logo picture
  • AP logo picture
  • Forbes logo picture
© Copyright 1997-2025
airSlate Legal Forms, Inc.
3720 Flowood Dr, Flowood, Mississippi 39232