نتایج جستجو برای: microtia
تعداد نتایج: 373 فیلتر نتایج به سال:
Golden har syndrome is a hereditary condition which is characterized by preauricular appendages, fistulas, and epibulbar dermoids. It not only involves the facial structures, but also includes renal, genitourinary, cardiac, and skeletal anomalies. The aetiology of the syndrome is not fully understood however many hypothesis have been proposed and described. The incidence varies from 1 in 3,500 ...
Chromosomal translocations affecting the 6p24 region have been associated with orofacial clefting. Here we present a female patient with cleft palate, severe growth retardation, developmental delay, frontal bossing, hypertelorism, antimongoloid slant, bilateral ptosis, flat nasal bridge, hypoplastic nasal alae, protruding upper lip, microretrognathia, bilateral, low set, and posteriorly rotated...
Congenital middle ear malformations are rare. Most part of them are usually associated with other malformations, such as aural atresia, microtia, and dysmorphic craniofacial features. A clinical case of a 24-year-old male with a right-sided conductive hearing loss since his childhood, without craniofacial malformation, is presented. He was proposed for exploratory tympanotomy under the suspicio...
OBJECTIVE To report a case of teratogenic effect of imatinib mesylate (IM) in a newborn, whose mother was suffering from chronic myelogenous leukemia and was treated with IM for 4 years, including during her pregnancy. CASE PRESENTATION AND INTERVENTION The newborn was diagnosed with microtia of the right ear, preauricular tag on the left side, absence of right depressor angular oris muscle, ...
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