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Biomedical subjects

E Viviente Rodríguez

Publications and source records attributed to E Viviente Rodríguez.

5 recordsLinked to original sources

[Supernumerary nostril].

Supernumerary nostril is an extremely rare congenital anomaly as a result of aberrant embryological development. Frequently it leads to a narrow cavity; in the end, opening into the nearest nasal cavity or just stops blindly after a short course. It can appear isolated or in association with other anomalies. Treatment is always surgical. We present a case of a triple nostril, associated to a congenital auricular hypoplasia and we also review the existing literature.

Aged↗

[Subjective satisfaction among patients with endoscopic surgery of paranasal sinuses].

The analysis of the subjective satisfaction degree in patients following endoscopic sinus surgery is a very important data to be studied in a ENT Hospital Departments. In a very high percentage of cases, the result was good or very good. No cases were reported as worse. Statistically the relationship between non-existence of post surgery complications and the rate of symptoms of smaller importance was logical. We would like to point out the importance in the meaningful association between the high degree of satisfaction with the presence of significant postoperative endoscopic findings.

Endoscopy↗

[Tissue engineering of cartilagenous tissue. Vital cryopreservation].

The characteristics of in vitro synthesized cartilage tissue using tissue engineering techniques before and after cryopreservation are described. We determined cell survival, growth of extracellular matrix (collagen and proteoglycan) using a computer analysis system, and characterized the cell phenotype with a monoclonal antibody specific for collagen type II. Chondrocytes maintained a differentiated phenotype with collagen and proteoglycan synthesis before and after cryopreservation.

Cartilage↗

[Familial mixed hearing loss associated with X chromosome and stapedial gusher].

Perilymphatic and/or CSF loss through the oval window during stapedectomy is called a gusher. This rare disorder is associated with X-linked progressive mixed hearing loss. It is related with mutations in the POU3F4 gene at locus DFN3 on Xq21. Our study of the cases seen in our department yielded information and clinical and radiological findings that could be useful for the clinical management, early diagnosis, and prevention of erroneous therapeutic indications.

Cochlea↗