BLEPHAROFYMOSIS, CLEFT PALATE AND CONGENITAL CARDIOPATHY ASSOCIATED WITH COGNITIVE DEFICIT, SYNDROME OF BLEPHAROFIMOSIS TYPE OHDO
Keywords:
blepharophimosis, cleft palate, intellectual disabilityAbstract
The Ohdo blepharophimosis syndrome is constituted by multiple congenital malformations, among them; Blepharophimosis, palpebral ptosis and dental hypoplasia, as well as retarded growth, intellectual and auditory disability. We present the case of an 11 - year - old schoolgirl with facial dysmorphia, including Blepharophimosis and Cleft Palate. It also presents antecedents of congenital heart disease and global developmental delay, of apparently healthy parents, who deny isonimia. The findings are discussed and the characteristics of the patient compared to the literature are compared. Fewer than 30 patients have been described worldwide, making the diagnosis of this syndrome an interesting finding. Diagnostic suspicion in intrauterine or early life is essential to reduce the impact on quality and life expectancy of patients, the importance of making an early diagnosis leads timely to relevant genetic and multidisciplinary advice.
Downloads
References
2. BieseckerG.TheOhdoblepharophimosissyndrome:athirdcase.J.Med.Genet, 1991; 28:131-134.
3. Jill Clayton-Smith, James O’Sullivan,1 Sarah Daly, Manchester (Europe) Published online:November10,2011.
4. Vulto-van Silfhout A, T de Vries B, Van Bon M, Hoischen A, Ruiterkamp-Versteeg M, et Al. Mutationsin MED 12 cause X-linked Ohdo syndrome. Am. J. Med. Genet. 2013; 92: 401-406
5. Say B, Barber N. Mental retardation with blepharophimosis. (Letter ) J .Med. Genet, 1987; 24:511only.
6. Day R, Beckett B, Donnai D, Fryer A, Heidenblad M. Clinical and genetic study of the Say/ Barber Biesecker Young-Simpson type of Ohdo syndrome. Clin. Genet, 2008; 74: 434-444.
7. Vignes NI. Epicanthus héréditarie. Rev Gen Ophtal, 1889; 8:438-42.
8. White, S. M., Ades, L. C., Amor, D., Liebelt, J., Bankier, A., Baker, E., Wilson, M., Savarirayan, R. Two further cases of Ohdo syndrome delineate the phenotypic variability of the condition. Clin. Dysmorph. 12:109-113,2003.
9. Lopes V, Guion-Almeida M. Ohdo syndrome: reportona Brazilian girl with additional findings. Clin.Genet, 1997; 51:268-270.
10. Mhanni A, Dawson A, Chudley, A. Vertical transmission of the Ohdo lepharophimosis syndrome .Am. J. Med. Genet,1998;77:144-145
Published
How to Cite
Issue
Section
Derechos del/de autor/es a partir del año de publicación
Esta obra está bajo la licencia:
Creative Commons Reconocimiento-NoComercial-CompartirIgual 4.0 Internacional (CC BY-NC-SA 4.0)
Las opiniones expresadas por los autores no necesariamente reflejan la postura del editor de la publicación ni de la UCLA. Se autoriza la reproducción total o parcial de los textos aquí publicados, siempre y cuando se cite la fuente completa y la dirección electrónica de esta revista. Los autores(as) tienen el derecho de utilizar sus artículos para cualquier propósito siempre y cuando se realice sin fines de lucro. Los autores(as) pueden publicar en internet o cualquier otro medio la versión final aprobada de su trabajo, luego que esta ha sido publicada en esta revista.