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Public Health Genomics and Precision Health Knowledge Base (v10.0)
PHGKB
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Public Health Genomics Branch
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CDC/NIH Web Information Database|Home|Public Health Genomics and Precision Health Knowledge Base (PHGKB)
CDC/NIH Web Information Database
CDC/NIH Information Database|Search|PHGKB
Last data update: Sep 03, 2024
. (Total: 8777 Documents)
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Records 1-28 (of 28 Records)
CDC/NIH Web Information
A Parent’s Guide to Genetics and Hearing Loss
CDC, 2023
Implementation of Population-Based Genetic Testing of Newborn Infants for Prediction of Hearing Loss in Ontario, Canada
CDC Webinar, April 19, 2023
Newborn Hearing Screening Can Improve Reading Skills
CDC, October 2021
Annual Data: Early Hearing Detection and Intervention (EHDI) Program
CDC, July 2021
Fulfilling the Promise - Ensuring the Success of Newborn Screening throughout Life
CDC, November 2019
Listen Up! Loud Noises Damage Hearing.
CDC, May 2019
Can your baby hear you say I love you?
CDC, May 2019
Information About Early Hearing Detection and Intervention (EHDI) State Programs
CDC Grand Rounds: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease
MMWR Weekly / August 25, 2017 / 66(33);888?890
Its Loud Out There: Hearing Health across the Lifespan
CDC Public Health Grand Rounds, June 20, 2017
Too Loud! For Too Long! Loud noises damage hearing
CDC Vital Signs, February 2017
Beyond the Blood Spot: Newborn Screening for Hearing Loss and Critical Congenital Heart Disease
CDC Public Health Grand Rounds, Septemeber 20, 2016
Protect Your Hearing, Promote Hearing Health
CDC Information: A Parent's Guide to Hearing Loss
CDC Information: About 1 out of 2 cases of hearing loss in babies is due to genetic causes
CDC Information: Doctors and Infant Hearing
How Children Can Be "Lost" to the Early Hearing System
Cerebellar ataxia, areflexia, pes cavus, optic atrophy and sensorinural hearing loss
From NCATS Genetic and Rare Diseases Information Center
Epiphyseal dysplasia hearing loss dysmorphism
From NCATS Genetic and Rare Diseases Information Center
Mastocytosis cutaneous with short stature conductive hearing loss and microtia
From NCATS Genetic and Rare Diseases Information Center
Nonsyndromic hereditary sensorineural hearing loss
From NCATS Genetic and Rare Diseases Information Center
Congenital ectodermal dysplasia with hearing loss
From NCATS Genetic and Rare Diseases Information Center
Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features
From NCATS Genetic and Rare Diseases Information Center
Camptodactyly, tall stature, and hearing loss syndrome
From NCATS Genetic and Rare Diseases Information Center
Choanal atresia-hearing loss-cardiac defects-craniofacial dysmorphism syndrome
From NCATS Genetic and Rare Diseases Information Center
Cleft palate, midfacial hypoplasia, triangular facies, and sensorineural hearing loss
From NCATS Genetic and Rare Diseases Information Center
Myopathy, mitochondrial progressive, with congenital cataract, hearing loss, and developmental delay
From NCATS Genetic and Rare Diseases Information Center
Autosomal recessive optic atrophy, hearing loss, and peripheral neuropathy
From NCATS Genetic and Rare Diseases Information Center
Sudden sensorineural hearing loss
From NCATS Genetic and Rare Diseases Information Center
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Page last reviewed:
Feb 1, 2024
Content source:
Public Health Genomics Branch in the Division of Blood Disorders and Public Health Genomics
,
National Center on Birth Defects and Developmental Disabilities
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