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Ocular phenotype and therapeutic interventions in keratitis-ichthyosis-deafness (KID) syndrome.
Mc Lean, Keri; Bignotti, Stefano; Callea, Michele; Cammarata-Scalisi, Francisco; Steger, Bernhard; Armstrong, David; Lagan, Maeve; Sinton, Janet; Semeraro, Francesco; Kaye, Stephen B; Romano, Vito; Willoughby, Colin E.
Affiliation
  • Mc Lean K; Department of Corneal and External Eye Diseases, St. Paul's Eye Unit, Royal Liverpool University Hospital, Liverpool, UK.
  • Bignotti S; Department of Eye and Vision Science, Institute of Life Course and Medical Science, University of Liverpool, Liverpool, UK.
  • Callea M; Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, Ophthalmology Clinic, University of Brescia, Brescia, Italy.
  • Cammarata-Scalisi F; Pediatric Dentistry and Special Dental Care Unit, Meyer Children's University Hospital IRCCS, Florence, Italy.
  • Steger B; Pediatrics Service, Regional Hospital of Antofagasta, Antofagasta, Chile.
  • Armstrong D; Department of Ophthalmology, Medical University of Innsbruck, Innsbruck, Austria.
  • Lagan M; Department of Ophthalmology, Royal Victoria Hospital, Belfast, UK.
  • Sinton J; Department of Ophthalmology, Royal Victoria Hospital, Belfast, UK.
  • Semeraro F; Department of Ophthalmology, Altnagelvin Area Hospital, Londonderry, UK.
  • Kaye SB; Department of Medical and Surgical Specialties, Radiological Sciences, and Public Health, Ophthalmology Clinic, University of Brescia, Brescia, Italy.
  • Romano V; Department of Corneal and External Eye Diseases, St. Paul's Eye Unit, Royal Liverpool University Hospital, Liverpool, UK.
  • Willoughby CE; Department of Eye and Vision Science, Institute of Life Course and Medical Science, University of Liverpool, Liverpool, UK.
Ophthalmic Genet ; 45(1): 16-22, 2024 Feb.
Article in En | MEDLINE | ID: mdl-37755702
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Corneal Diseases / Deafness / Ichthyosis / Keratitis Limits: Humans Language: En Journal: Ophthalmic Genet Journal subject: GENETICA MEDICA / OFTALMOLOGIA Year: 2024 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom
Fulltext
Add to My VHL
Print
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Corneal Diseases / Deafness / Ichthyosis / Keratitis Limits: Humans Language: En Journal: Ophthalmic Genet Journal subject: GENETICA MEDICA / OFTALMOLOGIA Year: 2024 Document type: Article Affiliation country: United kingdom Country of publication: United kingdom