Skip navigation

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you’ve safely connected to the .gov website. Share sensitive information only on official, secure websites.

Results 1 - 10 of 67 for Congenital deafness
  1. Congenital deafness with labyrinthine aplasia, microtia, and microdontia 
    Congenital deafness with labyrinthine aplasia, microtia, and microdontia (also called LAMM syndrome) is a condition that affects development of the ears and teeth. ...
    https://medlineplus.gov/...rinthine-aplasia-microtia-and-microdontia - Genetics
  2. Vohwinkel syndrome 
    ... no history of the disorder in their family. Congenital deafness with keratopachydermia and constrictions of fingers and toes ...
    https://medlineplus.gov/genetics/condition/vohwinkel-syndrome - Genetics
  3. FGF3 gene 
    ... the FGF3 gene cause a condition known as congenital deafness with labyrinthine aplasia, microtia, and microdontia (also known ...
    https://medlineplus.gov/genetics/gene/fgf3 - Genetics
  4. Jervell and Lange-Nielsen syndrome 
    ... syndrome Cardioauditory syndrome of Jervell and Lange-Nielsen Deafness, congenital, and functional heart disease Jervell-Lange Nielsen syndrome ...
    https://medlineplus.gov/.../jervell-and-lange-nielsen-syndrome - Genetics
  5. Hearing Disorders and Deafness (National Library of Medicine)  
    It's frustrating to be unable to hear well enough to enjoy talking with friends or family. Hearing disorders make it hard, but not impossible, to hear. They ...
    https://medlineplus.gov/hearingdisordersanddeafness.html - Health Topics
  6. SLC26A4 gene 
    ... as SLC26A4 Gene Mutations are Prominent Causes for Congenital Deafness. Cell Biochem Biophys. 2015 Sep;73(1):41- ... Identification of PENDRIN (SLC26A4) mutations in patients with congenital ... PDS causes non-syndromic recessive deafness. Nat Genet. 1998 Mar;18(3):215-7. ...
    https://medlineplus.gov/genetics/gene/slc26a4 - Genetics
  7. Ear Disorders (National Library of Medicine)  
    Your ear has three main parts: outer, middle and inner. You use all of them in hearing. Sound waves come in through your outer ear. They reach your middle ...
    https://medlineplus.gov/eardisorders.html - Health Topics
  8. Björnstad syndrome 
    ... JL, Bazex J, Schwarze HP. Pili torti with congenital deafness (Bjornstad syndrome): a case report. Pediatr Dermatol. 1999 ...
    https://medlineplus.gov/genetics/condition/bjornstad-syndrome - Genetics
  9. CACNA1D gene 
    ... function in a human channelopathy with bradycardia and congenital deafness. Nat Neurosci. 2011 Jan;14(1):77-84. ...
    https://medlineplus.gov/genetics/gene/cacna1d - Genetics
  10. Alport syndrome 
    ... others have only hematuria (thin basement membrane nephropathy). Congenital hereditary hematuria Hematuria-nephropathy-deafness syndrome Hematuric hereditary nephritis Hemorrhagic familial nephritis Hemorrhagic ...
    https://medlineplus.gov/genetics/condition/alport-syndrome - Genetics
previous · 1 · 2 · 3 · 4 · 5 · 6 · 7 · next