Results 61 to 70 of about 3,568 (145)

Choroidal thickness in Waardenburg syndrome

open access: yesGMS Ophthalmology Cases, 2019
Purpose: To assess the choroidal thickness in differently pigmented areas of the fundus in a 46-year-old female with Waardenburg syndrome. Methods: Retrospective, case review.
Rishi, Pukhraj   +4 more
doaj   +1 more source

The Waardenburg syndrome.

open access: yesSouth African medical journal = Suid-Afrikaanse tydskrif vir geneeskunde, 1998
Click on the link to view.
Scott, FP, van Beukering, JA
openaire   +2 more sources

Waardenburg Syndrome

open access: yesEar, Nose & Throat Journal, 1998
S, Smith, P, Kolodziej, A H, Olney
  +6 more sources

Waardinburg syndrome — inherited deafness with pigmentary involvement

open access: yesCurationis, 1979
The Waardenburg syndrome was first clearly defined in 1951. The major clinical importance lies in the fact that about 20% of affected individuals are deaf.
M.F. Macrae
doaj   +1 more source

Blue Eyed Boy

open access: yesOnline Journal of Health & Allied Sciences, 2015
We report a case of blue eyes of Waardenburg Syndrome, with findings of hypopigmentation on the posterior ...
Kamath MM, D Souza S, Sharma T
doaj  

Asymmetric severity of diabetic retinopathy in Waardenburg syndrome

open access: yesClinical Ophthalmology, 2011
Tomoyuki Kashima, Hideo Akiyama, Shoji KishiDepartment of Ophthalmology, Gunma University School of Medicine, Gunma 371-8511, JapanAbstract: A 30-year-old female patient was referred to our institution due to vitreous hemorrhage.
Kashima T, Akiyama H, Kishi S
doaj  

Waardenburg Syndrome and hirschsprung Disease in a child: A case report

open access: yesJournal of Pediatric Surgery Case Reports
Introduction: Waardenburg Syndrome (WS) type IV or Waardenburg-Shah Syndrome (WSS) is a genetic disorder characterized by sensorineural hearing loss, pigmentary defects of the hair and skin, heterochromia of the eyes, and Hirschsprung Disease (HD). There
Rajesh Prasad Sah   +5 more
doaj   +1 more source

Síndrome de Waardenburg. Variabilidad en una familia en Sandino, Pinar del Río, Cuba Waardenburg syndrome: variability in a Sandino family

open access: yesRevista de Ciencias Médicas de Pinar del Río, 2011
El síndrome de Waardenburg es una enfermedad infrecuente, autosómica y dominante que cursa con cierto grado de discapacidad cuando aparece la hipoacusia neurosensorial, sin embargo, se ha detectado en Sandino, Pinar del Río, Cuba, una familia con 26 ...
Fidel Castro Pérez   +4 more
doaj  

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