منابع مشابه
Frontonasal dysplasia associated with tetralogy of Fallot.
Three children with frontonasal dysplasia associated with tetralogy of Fallot are reported. All cases had true hypertelorism and a median nasal groove with absence of the nasal tip. There was no mental deficiency. The facial anomaly is a sporadic, non-genetic interference of the normal development of the face. This is the first report of frontonasal dysplasia associated with a cardiac defect. M...
متن کاملOptic disc anomalies and frontonasal dysplasia.
AIMS To document the optic disc abnormalities in patients with frontonasal dysplasia in association with basal encephalocele. METHODS Names and hospital numbers of patients with midline clefts were obtained from the ophthalmology and genetics database. Six patients were identified who had the following common findings: midline facial cleft with midline cleft lip and palate; hypertelorism; abs...
متن کاملMultiple pericallosal lipomas in two siblings with frontonasal dysplasia.
We report cases of two siblings with frontonasal dysplasia (FND) associated with multiple pericallosal lipomas in almost similar locations. In each sibling two separate curvilinear pericallosal lipomas were present-one in relation to the posterior part of the corpus callosum and the other in relation to the rostrum. To our knowledge, multiple pericallosal lipomas in association with FND have no...
متن کاملPrenatal diagnosis of frontonasal dysplasia with anterior encephalocele.
Frontonasal dysplasia is a rare congenital anomaly affecting the eyes, nose and forehead, and occurs sporadically in most of the cases. A 24-year-old woman was referred to our unit at 27 weeks gestation due to the preliminary diagnosis of encephalocele. The sagittal and axial sonography of the fetal face depicted a midline mass measuring 3.8 × 4.2 cm, projecting anteriorly between the fetal orb...
متن کاملFrontonasal dysplasia: clinical evaluation on audiological and brainstem electrophysiological profiles.
UNLABELLED Frontonasal dysplasia (FND) is a rare malformative complex affecting the frontal portion of the face, the eyes and the nose; it may occur singly or associated with other clinical signs. No systematic studies describing hearing in this condition were found. AIM To evaluate hearing sensitivity and sound stimulus conduction from cochlea to brainstem in patients with clinical signs of ...
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ژورنال
عنوان ژورنال: Otolaryngology–Head and Neck Surgery
سال: 2005
ISSN: 0194-5998,1097-6817
DOI: 10.1016/j.otohns.2005.06.019