Your browser doesn't support javascript.
loading
Oculoplastic approach to congenital cutis laxa syndrome.
Tas, Ahmet; Gundogan, Fatih C; Kocaturk, Tolga; Altun, Salih; Bayram, Yalçin.
Afiliación
  • Tas A; Department of Ophthalmology, Ankara Mevki Military Hospital, Altindag, Ankara, Turkey. anzhtas@hotmail.com
Aesthetic Plast Surg ; 37(2): 417-20, 2013 Apr.
Article en En | MEDLINE | ID: mdl-23443999
UNLABELLED: Cutis laxa is a rare congenital or acquired disorder of elastic tissue, characterized by loose skin with folds and multiple internal organ involvement, which may cause life-threatening complications. We present a patient with cutis laxa syndrome who had cross eyelids with esotropia. Bilateral lateral canthal tendon repositioning and bilateral medial rectus recession procedures were performed in a single session. The patient had acceptable eyelid and globe cosmesis after the procedure. LEVEL OF EVIDENCE IV: This journal requires that authors assign a level of evidence to each article. For a full description of these Evidence-Based Medicine ratings, please refer to the Table of Contents or the online Instructions to Authors http://www.springer.com/00266 .
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Procedimientos Quirúrgicos Oftalmológicos / Esotropía / Procedimientos de Cirugía Plástica / Cutis Laxo Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans Idioma: En Revista: Aesthetic Plast Surg Año: 2013 Tipo del documento: Article País de afiliación: Turquía

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Procedimientos Quirúrgicos Oftalmológicos / Esotropía / Procedimientos de Cirugía Plástica / Cutis Laxo Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Child / Female / Humans Idioma: En Revista: Aesthetic Plast Surg Año: 2013 Tipo del documento: Article País de afiliación: Turquía