ANOFTALMIA CONGENITA PDF

Vadala, P. Capozzi, M. Fortunato, A. Romanzo, F. Vadala, A. The authors describe a rare case of serohaemorrhagic monolateral cyst in a patient with congenital bilateral anophthalmia.

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Vadala, P. Capozzi, M. Fortunato, A. Romanzo, F. Vadala, A. The authors describe a rare case of serohaemorrhagic monolateral cyst in a patient with congenital bilateral anophthalmia.

Ocular examination shored bilateral anophthalmia with swelling palpebral superior in OS reducible digitopressure. N2 - The authors describe a rare case of serohaemorrhagic monolateral cyst in a patient with congenital bilateral anophthalmia.

AB - The authors describe a rare case of serohaemorrhagic monolateral cyst in a patient with congenital bilateral anophthalmia. Ospedale Pediatrico Bambino Gesu. Abstract The authors describe a rare case of serohaemorrhagic monolateral cyst in a patient with congenital bilateral anophthalmia.

Annali di Ottalmologia e Clinica Oculistica , 12 , Annali di Ottalmologia e Clinica Oculistica. In: Annali di Ottalmologia e Clinica Oculistica. Vadala and P. Capozzi and M. Fortunato and A. Romanzo and F. Vadala and A. AU - Capozzi, P. AU - Fortunato, M. AU - Romanzo, A. AU - Vadala, F. AU - Nuvoloni, A. PY - Y1 - N2 - The authors describe a rare case of serohaemorrhagic monolateral cyst in a patient with congenital bilateral anophthalmia.

Access to Document Link to publication in Scopus. Link to citation list in Scopus. A rare case of serohaemorrhagic monolateral cyst in a patient with congenital bilateral anophthalmia.

FRANCISCO REYES VILLAMIZAR DERECHO SOCIETARIO PDF

Heredofamilial Bilateral Anophthalmia

Genetics Home Reference: Leber congenital amaurosis. Molecular genetics of Leber congenital amaurosis. Hum Mol Directory of Open Access Journals Sweden. No ocurrieron complicaciones ni recurrencia tumoral a los seis meses de seguimiento.

DEMILITARISATION OF SIACHEN FILETYPE PDF

This report refers to a two years and nine months patient, carrier of clinical anophthalmia in her right eye associated with posterior coloboma in her left eye and systemic malformations. The abnormalities found have characteristics of congenital rubella syndrome CRS and congenital cytomegalovirus infection. It can also constitute genetic alteration, derive from other etiologies or present themselves without explanation. The mother manifested depressive symptoms, being shown to her specialized treatment. Further studies are needed to clarify the etiology of congenital eye malformations and the holistic cares to be valued during the relationship ophthalmologist-patient. Anophthalmia consists of a congenital or acquired malformation that is characterized by the absence of one or both eyes.

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