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Results 1 - 10 of 20 for Syndromic genetic hearing loss
  1. Vohwinkel syndrome is a disorder with classic and variant forms, both of which affect the skin.In the classic form of Vohwinkel syndrome, affected individuals ...
  2. Keratitis-ichthyosis-deafness (KID) syndrome is characterized by eye problems, skin abnormalities, and hearing loss.People with KID syndrome usually have keratitis, ...
  3. Palmoplantar keratoderma with deafness is a disorder characterized by skin abnormalities and hearing loss. Affected individuals develop unusually thick skin on the ...
  4. Bart-Pumphrey syndrome is characterized by nail and skin abnormalities and hearing loss.People with Bart-Pumphrey syndrome typically have a white discoloration ...
  5. Hystrix-like ichthyosis with deafness (HID) is a disorder characterized by dry, scaly skin (ichthyosis) and hearing loss that is usually profound. Hystrix-like ...
  6. ... cell is sufficient to cause the disorder. JWS ... Agochukwu NB, Solomon BD, Muenke M. Hearing loss in syndromic craniosynostoses: otologic manifestations and clinical findings. Int J ...
  7. ... described as syndromic. The most common form of syndromic retinitis ... genetic syndromes, including Bardet-Biedl syndrome; Refsum disease; and ...
  8. ... associated with nonsyndromic hearing loss can also cause syndromic forms of ... to genetic changes, hearing loss can result from environmental factors ...
  9. ... responsive megaloblastic anemia with diabetes mellitus and sensorineural hearing loss TRMA Genetic Testing Registry: Megaloblastic anemia, thiamine-responsive, with diabetes ...
  10. ... microtia, and microdontia Deafness with LAMM LAMM syndrome ... F, Wakil S, Alkayal F, Al-Saud H, Ramzan K, Al-Sayed M. Syndromic congenital sensorineural deafness, microtia and microdontia resulting from ...
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