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A case report of frontonasal dysplasia
International Journal of Pediatric Otorhinolaryngology, 2010The following report describes a case of mild frontonasal dysplasia, a rare congenital anomaly affecting the nose and frontal bone. Our patient was referred at 2 months of age with a complex nasal skin and tip deformity. This report outlines management of this patient and reviews the literature with regard to presentation and classification of this ...
J, Kean, S S M, Al-Busaidi, A A, Quaba
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Frontonasal dysplasia as an expression of holoprosencephaly
European Journal of Pediatrics, 1981A 3-year-old mildly retarded girl had frontonasal dysplasia. Computerized tomography showed brain changes compatible with a diagnosis of mild (pseudohemispheric) prosencephaly. The clinical features of frontonasal dysplasia may be an expression of (holo-)prosencephaly.
M, Roubicek, J, Spranger, S, Wende
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Experience with frontonasal dysplasia of varying severity
Journal of Pediatric Surgery, 1996Nine cases of frontonasal dysplasia were seen during an 8-year period. Seven were managed in the authors' institution, and the two adult relatives were referred to adult units. The age and sex distribution, the types of defects, and the family pedigree of an affected family are described.
I L, Qureshi, N U, Khan
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Frontonasal dysplasia or craniofrontonasal dysplasia and the Poland anomaly?
Clinical Genetics, 1990We describe a 10‐year‐old girl with features of a frontonasal dysplasia and a right‐sided Poland anomaly. As there has been one previous case report of pectoral muscle hypoplasia in association with craniofrontonasal dysplasia, the relationship between these two conditions is discussed.
W, Reardon +3 more
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A mild case of frontonasal dysplasia: the rhinologic perspective
International Journal of Pediatric Otorhinolaryngology, 2002Frontonasal dysplasia (FND) is a congenital malformation characterized by hypertelorism, broad nasion with a midline cleft in the bony dorsum, midline defect of the frontal bone, absence of the nasal tip, and deformities in the nasal alar region. The clinician should be aware of the mild forms of FND. We presented absence of crista galli in a mild case
Erkhan, Genç +2 more
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Prenatal Ultrasound Diagnosis of Frontonasal Dysplasia
Canadian Journal of Medical Sonography, 2018Sonographers are often exposed to rare fetal conditions. The following case study serves as an example. A healthy 28-year-old Caucasian female with a negative first trimester screen presented with complex facial and intracranial abnormalities at her routine detailed ultrasound.
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The spectrum of frontonasal dysplasia in an inbred pedigree
Clinical Genetics, 1980An inbred pedigree is described in which three members were affected with FND (Frontonasal Dysplasia). Two of these individuals werz products of a consanguineous mating with an inbreeding coefficient of F = 0.0391. The third affected individual (propositus), was born to a marriage in which the coefficient of inbreeding was 0.0742.
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Acromelic Frontonasal Dysplasia (Median Cleft Face Syndrome)
2017A 39-year-old woman, gravida 3, para 1, was referred to level II ultrasound at 16w5d of gestation with suspected midline facial anomaly, as detected at routine obstetrics scan. The parents were non-consanguineous, with uneventful medical and family history. First-trimester screening for Down syndrome showed a low risk for common trisomies.
Mario Lituania, Gabriele Tonni
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Integrative oncology: Addressing the global challenges of cancer prevention and treatment
Ca-A Cancer Journal for Clinicians, 2022Jun J Mao,, Msce +2 more
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