Hypertelorism
نویسندگان
چکیده
منابع مشابه
Nasal chondroma presenting as hypertelorism.
PURPOSE To report a rare case of nasal chondroma presenting as hypertelorism. CASE REPORT We report a case of a 16-year-old boy with a large calcified mass arising from the posterior nasal cavity presenting as hypertelorism. Surgical excision was done, and the histopathological examination revealed a chondroma. The hypertelorism resolved postoperatively. CONCLUSIONS Nasal chondroma may also...
متن کاملSurgical correction of grade III hypertelorism
Orbital hypertelorism is an increased distance between the bony orbits and can be caused by frontonasal malformations, craniofacial clefts, frontoethmoidal encephaloceles, glial tumors or dermoid cysts of the root of the nose, and various syndromic or chromosomal disorders. We report a series of 7 cases of hypertelorism that were treated in our hospital. The underlying causes in our series were...
متن کاملIris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome.
To sibs and an unrelated single patient have a combination of iris coloboma, ptosis, hypertelorism, broad nasal bridge, short stature, and mental retardation. The London Dysmorphology Database was used to determine whether this is a new syndrome.
متن کاملUmblical hernia, hypertelorism, sensorineural deafness: Is it Donnai–Barrow syndrome?
Introduction: Donnai–Barrow syndrome is a rare autosomal recessive disorder first described in 1993 and characterized by diaphragmatic hernia, hypertelorism, agenesis of the corpus callosum and deafness. Case Report: A 23yearold female with clinical features similar to Turner patients were sent to our department by cardiology department. The main features were umblical hernia, hypertelorism (...
متن کاملIris coloboma, ptosis, hypertelorism, and mental retardation: a new syndrome possibly localised on chromosome 2.
A patient with a phenotype resembling that of three children recently reported is described. His karyotype shows a pericentric inversion of chromosome 2, very similar to another child previously reported. We discuss the possibility that all these cases constitute a distinct syndrome.
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ژورنال
عنوان ژورنال: Indian Journal of Plastic Surgery
سال: 2014
ISSN: 0970-0358,1998-376X
DOI: 10.4103/0970-0358.146572